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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1415266Generated: November 3, 2026

Acetic Anhydride → 6-Formyloxy-1-methyl-4-methylen-2,3,3a,4,5,6,7,8-octahydroazulene

https://huagongshe.com/reaction/1415266

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium CarbonateHCID 10340—
Reactant3-Methyl-8-methylidene-1,2,4,5,6,7,8,8a-octahydroazulen-6-olHCID 21434886—
CatalystPyridineHCID 1049—
SolventFormic AcidHCID 284—
Product6-Formyloxy-1-methyl-4-methylen-2,3,3a,4,5,6,7,8-octahydroazuleneHCID 2143490887.4%

Reaction Steps

2.67 g of 6-hydroxy-1-methyl-4-methylen-2,3,3a,4,5,6,7,8-octahydroazulene were treated at 0° firstly with half of a mixture of 4.08 g of acetic anhydride, 1.84 g of formic acid and 37 mg of pyridine. The mixture was stirred for 24 hours at room temperature and with exclusion of light. Then the other half of the reagent was added and the mixture stirred for further 24 hours. The solution was poured on to a mixture of ice and sodium carbonate and worked up in a conventional manner. The crude product so obtained (3.18 g) was distilled under high vacuum and yielded 2.70 g (87%) of pure 6-formyloxy-1-methyl-4-methylen-2,3,3a,4,5,6,7,8-octahydroazulene; b.p.0.005 50°; IR(film): νmax = 3120, 1728, 1645, 1460/45, 1190/82, 1015/1000, 905/900 cm-1. The compound smells woody, cedar-like, slightly ionone-like.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04003951
Source datasetuspto-grants-1977_01
ORD IDord-3d15739760484fbeb883224e0b6dbba4
Source noteuspto-grants-1977_01