Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 483897Generated: October 29, 2026

Acetic Anhydride → HCID 14631299, compound

https://huagongshe.com/reaction/483897

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantCyclohexanone, 4-hydroxy-2,2,6-trimethyl-, (4R,6R)-HCID 10313234—
SolventPyridineHCID 1049—
ProductHCID 14631299HCID 1463129999.4%

Reaction Steps

300 g of (4R, 6R)-4-hydroxy-2,2,6-trimethylcyclohexanone were dissolved in 154.7 ml of pyridine. The solution was treated dropwise at -3° C. to 0° C. within 10 minutes with 1.2 l of acetic anhydride and then stirred at room temperature for a further 4.25 hours. The reaction mixture was subsequently concentrated on a rotary evaporator at 60° C./16 mbar, whereby there were obtained 394.7 g of crude product as a yellow oil. Distillation of the crude product gave at about 95° C./0.07 mbar 378.4 g (99.4%) of (4R, 6R)-4-acetoxy-2,2,6-trimethylcyclohexanone as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05227507
Source datasetuspto-grants-1993_07
ORD IDord-5e21179d959342439294bf0e246e2ba0
Source noteuspto-grants-1993_07