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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 727794Generated: October 30, 2026

Triethylamine → HCID 67924837, compound

https://huagongshe.com/reaction/727794

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzyl chloroformateHCID 10387—
ReactantHCID 67924832HCID 67924832—
SolventDichloromethaneHCID 6344—
ProductHCID 67924837HCID 67924837—

Reaction Steps

4.18 ml of benzyl chloroformate are added at a temperature of 2° to 5° to a solution of 5.28 ml of triethylamine and 6.3 g of (2S,3S)-1-amino-3-BOC-amino-4-cyclohexyl-2-butanol in 120 ml of dichloromethane, and the solution obtained is stirred for 30 minutes at room temperature. The solution is then diluted with dichloromethane and washed with 0.25N hydrochloric acid, saturated aqueous sodium bicarbonate solution and water. The organic phase is dried over sodium sulphate and evaporated under vacuum. Chromatography of the residue on silica gel using toluene/ethyl acetate (3:1) as the eluant yields (2S,3S)-3-BOC-amino-1-Cbz-amino-4-cyclohexyl-2-butanol as a slightly yellowish oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05045537
Source datasetuspto-grants-1991_09
ORD IDord-e1ca9e5844454b789ea98cef3030dd0e
Source noteuspto-grants-1991_09