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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2290979Generated: October 29, 2026

Triethylamine → HCID 70419999, compound

https://huagongshe.com/reaction/2290979

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSulfuryl chlorideHCID 24648—
ReactantDibenzylphosphinic chlorideHCID 12809684—
ReactantDibenzylphosphiteHCID 21904359—
ReactantHCID 70420509HCID 70420509—
SolventChloroformHCID 6212—
ProductHCID 70419999HCID 70419999—

Reaction Conditions

Temperature0 °C

Reaction Steps

2g of L-phenylalanine-glycine methyl ester hydrochloride (7.4 mmoles) are put in suspension in 20 ml of anhydrous chloroform. 1.50 g of triethylamine (15 mmoles) are added. The solid enters into solution. The solution is cooled to 0° C. and 2.17 g (7.4 mmoles) of dibenzyl phosphoryl chloride freshly prepared from dibenzyl phosphite and sulfuryl chloride are added while stirring for 30 minutes. The mixture is allowed to stand for 20 hours at room temperature. The precipitate formed is filtered and the filtrate is washed in succession with 30 ml of 1N HCl, 20 ml of water, 20 ml of 10% bicarbonate, then 2×30 ml of water. The organic solution is dried on anhydrous Na2SO4 and evaporated under a vacuum. A pale yellow solid is obtained which is recrystallized in ethyl acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04618708
Source datasetuspto-grants-1986_10
ORD IDord-49fd97c1459141acbc66590fda25e43c
Source noteuspto-grants-1986_10