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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6476Generated: October 23, 2026

Dichloromethane → glycyl-D-alanine benzyl ester hydrochloride

https://huagongshe.com/en/reaction/6476

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriethylamineHCID 8471—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantN-(tert-butoxycarbonyl)glycineHCID 78288—
ReactantD-Alanine, phenylmethyl ester, 4-methylbenzenesulfonate (1:1)HCID 2802425—
Productglycyl-D-alanine benzyl ester hydrochlorideHCID 6778873070%

Reaction Steps

To a cold (0° C.) solution of 100 ml. methylene chloride containing 10 g. (57 mmol) of N-t-butyloxycarbonylglycine, 20 g. (57 mmol) of D-alanine benzyl ester p-toluene sulfonic acid salt and 5.77 g. (57 mmol) of triethylamine was added 12.3 g. (60 mmol) of dicyclohexylcarbodiimide and the resulting action mixture allowed to warm to room temperature. After 18 hours the mixture was filtered and the filtrate concentrated in vacuo. The residue was dissolved in 200 ml. of ethyl acetate and the organic layer washed with 2.5% hydrochloric acid, water, a saturated sodium bicarbonate solution and a brine solution. The organic layer was separated, dried over magnesium sulfate and evaporated under reduced pressure. To the resulting oil 200 ml. of dioxane saturated with hydrogen chloride was added. After 30 minutes 40 ml. of diethyl ether was added and the product filtered under nitrogen, 10.9 g. (70% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05248820
Source datasetuspto-grants-1993_09
ORD IDord-f4cc62040f7c42ea8b1be3806e91e5ff
Source noteuspto-grants-1993_09