Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1432921Generated: November 1, 2026

Propargyl bromide → 2-Benzyloxycarbonylamino-3-(prop-2-ynylamino)-propionic acid methyl ester

https://huagongshe.com/reaction/1432921

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
ReactantTriethylamineHCID 8471—
ReactantMethyl 3-amino-2-(phenylmethoxycarbonylamino)propanoate;hydrochlorideHCID 21584654—
SolventTetrahydrofuranHCID 8028—
Product2-Benzyloxycarbonylamino-3-(prop-2-ynylamino)-propionic acid methyl esterHCID 54423640—

Reaction Conditions

Temperature50 °C

Reaction Steps

Propargyl bromide (1.6 mL, 14.4 mmol) is added to a solution of 3-amino-2-benzyloxycarbonylamino-propionic acid methyl ester hydrochloride (4.0 g, 13.9 mmol) and triethylamine (4.1 mL, 29.4 mmol) in THF (46 mL). The resulting mixture is heated to 50° C. and stirred overnight then cooled to RT and concentrated in vacuo. The crude residue is diluted with methylene chloride, washed with saturated NaHCO3 and brine then the organic layer is dried over MgSO4, filtered and concentrated in vacuo. The crude material (4.0 g) is taken on to the subsequent step without further purification. 1H NMR (CDCl3, 300 MHz) δ7.25-7.30 (m, 5H), 5.75 (bs, 1H), 5.20 (s, 2H), 4.45 (bs, 1H), 3.80 (s, 3H), 3.75 (m, 1H), 3.31 (s, 2H), 3.08 (dd, 1H), 2.98 (dd, 1H), 2.20 (t, 1H). EI MS, [M+H]+=291.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612075B2
Source datasetuspto-grants-2009_11
ORD IDord-03b821690b30428bb9fe4c28ee0ed4d3
Source noteuspto-grants-2009_11