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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412008Generated: October 29, 2026

2-Bromoethanol → HCID 15907411, compound

https://huagongshe.com/reaction/412008

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromoethanolHCID 10898—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 23700149HCID 23700149—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 15907411HCID 1590741121.9%

Reaction Conditions

Temperature25 °C

Reaction Steps

N-Benzyl-N-methyl glycine potassium salt (2.00 g, 11.16 mmol) and 2-Bromo ethanol (2.48 g, 17.86 mmol) was suspended in 20 mL of dichloromethane. To this solution was added 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (6.40 g, 33.5 mmol) and 4-(dimethylamino)pyridine (1.00 g) and the reaction was stirred at 25° C. overnight. The mixture was diluted with 40 mL of dichloromethane, and was washed with water (1×60 mL), saturated sodium bicarbonate solution (2×60 mL), and brine (1×60 mL). The organic phase was then dried over magnesium sulfate, and filtered through a pad of Celite. Evaporation of the solvent in vacuo afforded an oil, which was purified on silica gel eluting with ethyl acetate to afford N-Benzyl-N-methyl glycine 2-bromoethyl ester as an oil (0.70 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06562824B2
Source datasetuspto-grants-2003_05
ORD IDord-b8d17141b12347d7b2ace0c8ad9a45d9
Source noteuspto-grants-2003_05