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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013328Generated: October 27, 2026

Triethylamine → 8-Tert-butyl-1-oxa-2-azaspiro[4.5]dec-2-ene-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1013328

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantCyclohexane, 1-(1,1-dimethylethyl)-4-methylene-HCID 139425—
ReactantEthyl chloro(hydroximino)acetateHCID 6816376—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product8-Tert-butyl-1-oxa-2-azaspiro[4.5]dec-2-ene-3-carboxylic acid ethyl esterHCID 57951451—

Reaction Steps

A solution of 2-chloro-2-hydroxyiminoacetic acid ethyl ester (2.2 g, 14.6 mmol) in DCM (20 ml) was slowly added dropwise at 0° C. to a solution of 1-tert-butyl-4-methylenecyclohexane (740 mg, 4.86 mmol) in DCM (20 ml). Subsequently, a solution of triethylamine (1.5 ml) in DCM (10 ml) was slowly added dropwise at 0° C. and the resulting mixture was stirred overnight at RT. The reaction mixture was diluted with water. The aqueous phase was extracted several times with DMC. The combined organic phases were dried and the solvent was removed under vacuum. After purification of the residue (silica gel, hexane/ether 2:1) by column chromatography, the desired product 8-tert-butyl-1-oxa-2-azaspiro[4.5]dec-2-ene-3-carboxylic acid ethyl ester was obtained as a yellowish liquid (1.21 g, 93% of the theoretical amount).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981883B2
Source datasetuspto-grants-2011_07
ORD IDord-566452ae43d8471fbbe1319fa0c3a372
Source noteuspto-grants-2011_07