Patent US3931291A successfully refreshed from Google Patents.
US3931291A
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Preparation of optically active allethrorone via allethronyl acid phthalate
Assignee: Sumitomo Chemical Co Ltd
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Filing: 1974-03-22
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Granted: 1976-01-06
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Expires: 1994-03-22
Abstract
Abstract Optically active allethronyl acid phthalate is prepared by reacting (±)-allethronyl acid phthalate of the formula ##SPC1## With an optically active amine from the group of α-phenylethylamine of the formula, ##SPC2## α-phenyl-β-p-tolylethylamine of the formula ##SPC3## Threo-2-dimethylamino-1-(p-nitrophenyl)-1,3-propanediol of the formula ##SPC4## And naphthylethylamine of the formula ##SPC5## To form diastereomeric salts thereof, and decomposing the resolved salt to obtain the optically active allethronyl acid phthalate.
Inventors
- 👤 Fukashi Horiuchi
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-11-07 16:27
CPC Classifications
C; C07; C07B; C07B53/00; C07C; C07C67/00; C07C69/00; C07C69/76; C07C69/80; C07B2200/00; C07B2200/07
Claims Analysis
Total Claims: 3
Claim 1
Independent Claim
134 words
A method for preparing optically active allethronyl acid phthalate, which comprises reacting (±)-allethronyl acid phthalate of the formula ##SPC12## with an optically active amine selected from the group consisting of α-phenylethylamine of the formula ##SPC13## α-phenyl-β-p-tolylethylamine of the formula, ##SPC14## threo-2-dimethylamino-1-(p-nitrophenyl)-1,3-propanediol of the formula, ##SPC15## and naphthylethylamine of the formula ##SPC16## in the presence of a solvent selected from the group consisting of benzene, toluene, hexane, chloroform, tetrachloromethane, chlorobenzene, dichloroethane, tetrachloroethylene, ethylether, isopropylether, acetone, methylethyl ketone, methylisobutyl ketone, diisobutyl ketone, ethyl acetate, methanol, ethanol, propanol, isopropyl alcohol, a mixture thereof and an aqueous mixture thereof, the ratio of the optical active amine being 0.5 to 1.5 mole to 1 mole of the allethronyl acid phthalate, to form a diastereomeric salt thereof, and decomposing the resolved salt to obtain the optically active allethronyl acid phthalate.
Claim 2
Independent Claim
134 words
A method for preparing optically active allethronyl acid phthalate, which comprises reacting (±)-allethronyl acid phthalate of the formula ##SPC12## with an optically active amine selected from the group consisting of α-phenylethylamine of the formula ##SPC13## α-phenyl-β-p-tolylethylamine of the formula, ##SPC14## threo-2-dimethylamino-1-(p-nitrophenyl)-1,3-propanediol of the formula, ##SPC15## and naphthylethylamine of the formula ##SPC16## in the presence of a solvent selected from the group consisting of benzene, toluene, hexane, chloroform, tetrachloromethane, chlorobenzene, dichloroethane, tetrachloroethylene, ethylether, isopropylether, acetone, methylethyl ketone, methylisobutyl ketone, diisobutyl ketone, ethyl acetate, methanol, ethanol, propanol, isopropyl alcohol, a mixture thereof and an aqueous mixture thereof, the ratio of the optical active amine being 0.5 to 1.5 mole to 1 mole of the allethronyl acid phthalate, to form a diastereomeric salt thereof, and decomposing the resolved salt to obtain the optically active allethronyl acid phthalate.
Claim 3
Dependent Claim
17 words
A method according to claim 1, wherein the diastereomeric salt is decomposed with an acid or alkali.
References Cited (Backward Citations)
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1979-01-05 | 1979-07-07 | 1980-01-06 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1983-01-05 | 1983-07-07 | 1984-01-06 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1987-01-05 | 1987-07-07 | 1988-01-06 | $7700.00 | Window Closed / Lapsed |