Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | Acetic acid 10-acetoxymethyl-anthracen-9-ylmethyl ester | HCID 613145 | — |
| 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 11 l. of acetic anhydride is refluxed acetic a rate to maintain a steady distillation of acetic acid from the reaction through a relix-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 | USRE029469 |
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| Source dataset | uspto-grants-1977_11 |
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| ORD ID | ord-b9aa4ca9b7af4a1cbee46776bb080ba3 |
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| Source note | uspto-grants-1977_11 |
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