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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276124Generated: October 29, 2026

Triethylamine → HCID 12051603, compound

https://huagongshe.com/reaction/276124

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 22730904HCID 22730904—
SolventDichloromethaneHCID 6344—
ProductHCID 12051603HCID 1205160399.8%

Reaction Steps

A solution of methanesulfonyl chloride (6.1 mL, 78.5 mmol) in dichloromethane (50 mL) was added to a stirring solution of ethyl 3-hydroxy 4-oxo-6-methyl-2,3,4,5,6,7-hexahydrobenzofuran-3-carboxylic acid (18.48 g, 76 mmol) and triethylamine (21.4 mL, 154 mmol) in dichloromethane (150 mL) at 0° C. The mixture was allowed to reach ambient temperature, stirred for 2 hours, then poured into aqueous 1N sodium hydroxide and extracted with ethyl acetate. The organic layer was washed with brine, dried over magnesium sulfate, filtered, and concentrated in vacuo to give ethyl 4-oxo-6-methyl-4,5,6,7-tetrahydrobenzofuran-3-carboxylate (16.86 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06353109B2
Source datasetuspto-grants-2002_03
ORD IDord-773fa134ce8d44f5a832923fa2a557b6
Source noteuspto-grants-2002_03