HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 66973Generated: October 29, 2026
Acetic Anhydride → HCID 20465612, compound
https://huagongshe.com/reaction/66973
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | 2-(5-Hydroxypentyl)cyclopentan-1-one | HCID 20465518 | — |
| Reactant | 2-(5-Hydroxypentyl)cyclopentanone 2-(5-acetoxypentyl)-cyclopentanone | HCID 86732937 | — |
| Product | HCID 20465612 | HCID 20465612 | — |
Reaction Steps
A solution of 400 g. (2.04 moles) of a mixture of 2-(5-hydroxypentyl)cyclopentanone and 2-(5-acetoxypentyl)cyclopentanone (Example 55) and 4.0 g. of p-toluenesulfonic acid monohydrate in 1 l. of acetic anhydride is refluxed at a rate to maintain a steady distillation of acetic acid from the reaction through a helix-packed fractionation column. The reaction is continued with the addition of acetic anhydride to maintain a constant volume until complete conversion of starting materials to product is evident. The mixture is cooled and partitioned between 2 l. of hexane and 3 l. of cold water containing solid sodium bicarbonate to maintain a neutral pH. The organic phase is washed with saturated brine. dried (MgSO4), and evaporated to yield 452 g. of an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04343949 |
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| Source dataset | uspto-grants-1982_08 |
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| ORD ID | ord-4f2359555168413fb3d83b5c45b8f9c5 |
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| Source note | uspto-grants-1982_08 |
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