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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 649243Generated: October 29, 2026

Triethylamine → HCID 70419999, compound

https://huagongshe.com/reaction/649243

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

2 g 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 numberUS04738803
Source datasetuspto-grants-1988_04
ORD IDord-d57968be17c94004a1cce1ebea2dbe29
Source noteuspto-grants-1988_04