Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1382907Generated: October 31, 2026

Triethylamine → HCID 178439176, compound

https://huagongshe.com/reaction/1382907

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantIsobutyl chloroformateHCID 62365—
Reactant(E)-p-(2-(4,4-Dimethylchroman-6-yl)propenyl)benzoic acidHCID 6366138—
ReactantHCID 178509299HCID 178509299—
SolventChloroformHCID 6212—
SolventDimethylformamideHCID 6228—
Solventchloroform N,N-dimethylformamideHCID 21754633—
ProductHCID 178439176HCID 178439176—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a stirred solution of 0.5 g (1.55 mmole) of 4-[(E)-2-(4,4-dimethyl-6-chromanyl)-2-methylvinyl]benzoic acid in 20 ml of chloroform-N,N-dimethylformamide (1:1) at -25° C., under nitrogen, was added 0.17 g of triethylamine followed by 0.23 g (1.7 mmole) of isobutyl chloroformate. Stirring was continued for 15 minutes at -25° C. and then a solution of 0.177 g (1.7 mmole) of 5-aminotetrazole in 4 ml of N,N-dimethylformamide was added dropwise during 2 minutes. Stirring was continued for 1 hour as the reaction mixture was allowed to warm to 25° C. The reaction mixture was then diluted with 50 ml of chloroform and washed with 50 ml of 1N hydrochloric acid. The insoluble material was recovered by filtration to give a first crop of the title compound. The layers were then separated and the chloroform layer was washed with 1N hydrochloric acid followed by saturated sodium chloride, dried (MgSO4) and concentrated in vacuo. The residue was triturated under hot chloroform and the insoluble material was collected by filtration to give a second crop of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04808597
Source datasetuspto-grants-1989_02
ORD IDord-16b79f462cd2454c9247776bd889dcc7
Source noteuspto-grants-1989_02