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US4347386A Expired / Lapsed US ⏱️ 0.0 years remaining

Process for preparing cyclopentenolones

Assignee: Sumitomo Chemical Co Ltd
•
Filing: 1981-04-22
•
Granted: 1982-08-31
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Expires: 2001-04-22
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Abstract

Abstract A process for preparing cyclopentenolones in good yields which comprises treating a 4-hydroxy-4-R2-5-R1-2-cyclopentenone of the formula: <IMAGE> wherein R1 is an alkyl group having not more than 6 carbon atoms, an alkenyl group having not more than 6 carbon atoms, an alkynyl group having not more than 6 carbon atoms or a group of the formula: <IMAGE> (in which R3 is hydrogen, methyl or halogen) and R2 is a hydrogen atom or a methyl group, provided that when R2 is hydrogen, R1 is neither alpha -methylallyl nor alpha -methylpropargyl, in an aqueous medium in the presence or absence of a metal salt at a temperature of 20 DEG to 200 DEG C. to give the corresponding 2-R1-3-R2-4-hydroxy-2-cyclopentenone of the formula: <IMAGE> wherein R1 and R2 are each as defined above.

Inventors

  • 👤 Kenji Saito
  • 👤 Hiroshi Yamachika

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-07 17:26
CPC Classifications
C; C07; C07C; C07C45/00; C07C45/61; C07C45/67

Claims Analysis

Total Claims: 5
Claim 1
Independent Claim 121 words
A process for preparing cyclopentenolones which comprises treating a 4-hydroxy-4-R 2 -5-R 1 -2-cyclopentenone of the formula: ##STR13## wherein R 1 is an alkyl group having not more than 6 carbon atoms, an alkenyl group having not more than 6 carbon atoms, an alkynyl group having not more than 6 carbon atoms or a group of the formula: ##STR14## in which R 3 is hydrogen, methyl or halogen and R 2 is a hydrogen atom or a methyl group, provided that when R 2 is hydrogen, R 1 is neither α-methylallyl nor α-methylpropargyl, in an aqueous medium to give the corresponding 2-R 1 -3-R 2 -4-hydroxy-2-cyclopentenone of the formula: ##STR15## wherein R 1 and R 2 are each as defined above.
Claim 2
Dependent Claim 121 words
A process for preparing cyclopentenolones which comprises treating a 4-hydroxy-4-R 2 -5-R 1 -2-cyclopentenone of the formula: ##STR13## wherein R 1 is an alkyl group having not more than 6 carbon atoms, an alkenyl group having not more than 6 carbon atoms, an alkynyl group having not more than 6 carbon atoms or a group of the formula: ##STR14## in which R 3 is hydrogen, methyl or halogen and R 2 is a hydrogen atom or a methyl group, provided that when R 2 is hydrogen, R 1 is neither α-methylallyl nor α-methylpropargyl, in an aqueous medium to give the corresponding 2-R 1 -3-R 2 -4-hydroxy-2-cyclopentenone of the formula: ##STR15## wherein R 1 and R 2 are each as defined above.
Claim 3
Dependent Claim 20 words
The process according to claim 1, wherein the treatment is carried out at a temperature of 20° to 200° C.
Claim 4
Dependent Claim 20 words
The process according to claim 1, wherein the treatment is carried out at a temperature of 120° to 200° C.
Claim 5
Dependent Claim 19 words
The process according to claim 1, wherein the treatment is carried out in the presence of a metal salt.

References Cited (Backward Citations)

US3981920A Cited
US3932510A Cited
US3932511A Cited
US4234516A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1985-08-30 1986-03-01 1986-08-31 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1989-08-30 1990-03-01 1990-08-31 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1993-08-30 1994-03-01 1994-08-31 $7700.00 Window Closed / Lapsed

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