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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2070548Generated: October 30, 2026

Triethylamine → 6-Methanesulfonyloxy-spiro[4.5]decane-7-carboxylic acid methyl ester

https://huagongshe.com/reaction/2070548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium BicarbonateHCID 516892—
Reactant6-Hydroxy-spiro[4.5]decane-7-carboxylic acid methyl esterHCID 57771536—
SolventChloroformHCID 6212—
Product6-Methanesulfonyloxy-spiro[4.5]decane-7-carboxylic acid methyl esterHCID 57771563—

Reaction Steps

To a solution of 6-hydroxy-spiro[4.5]decane-7-carboxylic acid methyl ester (10.1 g) obtained in Step 3 and triethylamine (19.9 mL) in chloroform (100 mL) was added dropwise methanesulfonyl chloride (5.2 mL) under ice-cooling, followed by stirring the reaction mixture at room temperature for 2 hours. Then, after addition of triethylamine (10 mL), the reaction mixture was stirred at room temperature for 30 minutes. After ice-cooling, ice-cold water (30 mL) and saturated aqueous sodium bicarbonate solution (50 mL) were added to the reaction mixture, followed by separation of the organic layer. The organic layer was washed with saturated brine, dried and concentrated to give a crude 6-methanesulfonyloxy-spiro[4.5]decane-7-carboxylic acid methyl ester (22 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299296B2
Source datasetuspto-grants-2012_10
ORD IDord-de9ee4fd15044adaa9116f8386be08c0
Source noteuspto-grants-2012_10