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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1805225Generated: November 2, 2026

Triethylamine → HCID 86653290, compound

https://huagongshe.com/reaction/1805225

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTriphosgeneHCID 94429—
ReactantHCID 66705807HCID 66705807—
SolventDichloromethaneHCID 6344—
ProductHCID 86653290HCID 86653290253.7%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a stirred suspension of (S)-4-[2-(4-amino-phenyl)-ethyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester (600 mg, example 14 (b)) in dichloromethane (10 ml) were added sequentially triethylamine (0.52 ml) and triphosgene (206 mg) and the mixture was heated at 50° C. for 18 h. The mixture was then concentrated in vacuo and to the residue was added diethyl ether. After stirring for 10 min at room temperature the resulting crystals were removed by filtration. The filtrate was concentrated in vacuo to give (S)-4-[2-(4-isocyanato-phenyl)-ethyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester (610 mg, 94%) as a yellow oil which was used immediately in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354441B2
Source datasetuspto-grants-2013_01
ORD IDord-a9f1e855f8ef403fb9c1239763a2931c
Source noteuspto-grants-2013_01