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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1194789Generated: October 30, 2026

HCID 23049242, compound → (3,3,6,6-Tetramethylcyclohex-1-en-1-yl)acetic acid

https://huagongshe.com/reaction/1194789

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 23049242HCID 23049242—
CatalystSodium amalgamHCID 9837419—
SolventEthanolHCID 702—
Product(3,3,6,6-Tetramethylcyclohex-1-en-1-yl)acetic acidHCID 2304923284.9%

Reaction Steps

20.6 g of 3,3,6,6-tetramethyl-α-(phenylsulphonyl)-1-cyclohexen-1-acetic acid are dissolved in 800 ml of ethanol and the solution is treated at 0° C. with 107.1 g of sodium amalgam (5%). The mixture is stirred at room temperature for 4.5 hours, the solution is decanted off from the mercury, acidified with 2N hydrochloric acid and extracted with ethyl acetate. The organic phase is washed with water, dried, evaporated and filtered over silica gel (eluting agent hexane/ether 1:1). After recrystallization from hexane, there are obtained 10.2 g of 3,3,6,6-tetramethyl-1-cyclohexen-1-acetic acid in the form of colorless crystals, m.p. 50°-54° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04816476
Source datasetuspto-grants-1989_03
ORD IDord-78b71e18fdee4b43a318e683fa9f9842
Source noteuspto-grants-1989_03