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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1185479Generated: November 3, 2026

Triethylamine → HCID 68600866, compound

https://huagongshe.com/reaction/1185479

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantButyl chloroformateHCID 61140—
ReactantHCID 68599591HCID 68599591—
SolventDichloromethaneHCID 6344—
ProductHCID 68600866HCID 68600866—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2 g of Azetidin-3-yl-carbamic acid benzyl ester trifluoroacetate (prepared by standard protection and deprotection procedures from 3-Amino-azetidine-1-carboxylic acid tert-butyl ester) in 10 ml of DCM, 1.9 g of triethylamine was added and the mixture was cooled to 0° C. Then, 938 mg of butyl chloroformate was slowly added. After the addition was completed the reaction mixture was allowed to warm to RT and to stir for 1 h. Then, 200 ml of DCM was added and the organic phase was washed two times with 0.1M aqueous hydrochloric acid and the with saturated aqueous sodium hydrogen carbonate solution. The organic phase was dried over MgSO4 and the solvents were removed under reduced pressure. The crude product was purified by chromatography on silica gel eluting with a gradient of n-heptane/ethyl acetate. The fractions containing the product were combined and the solvent evaporated under reduced pressure. Yield: 1.4 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08669266B2
Source datasetuspto-grants-2014_03
ORD IDord-76d43405866a44a796a6d50962dcec0d
Source noteuspto-grants-2014_03