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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 615951Generated: October 30, 2026

Acetic Anhydride → 2-Acetoxy-2,3-dihydro-3,3-dimethylbenzofuran-5-yl methanesulphonate

https://huagongshe.com/reaction/615951

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
Reactant(2-Hydroxy-3,3-dimethyl-2H-1-benzofuran-5-yl) methanesulfonateHCID 536079—
SolventDiethyl EtherHCID 3283—
Product2-Acetoxy-2,3-dihydro-3,3-dimethylbenzofuran-5-yl methanesulphonateHCID 13088532—

Reaction Steps

A solution of 2-hydroxy-2,3-dihydro-3,3-dimethylbenzofuran-5-yl methanesulphonate (5 parts) in ether (85 parts) was treated with triethylamine (2.2 parts) and acetic anhydride (2.3 parts) at 10° C and allowed to stand for 4 hours. The solution was then diluted with light petroleum (80 parts) and filtered. The filtrate was evaporated to give an oil which solidified. This was recrystallised from a mixture of chloroform and petroleum to give 2-acetoxy-2,3-dihydro-3,3-dimethylbenzofuran-5-yl methanesulphonate (2.5 parts), melting point 84°-85° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04072495
Source datasetuspto-grants-1978_02
ORD IDord-4e3450c4964e4744b58984b61d1e29d7
Source noteuspto-grants-1978_02