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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333100Generated: October 31, 2026

Ethyl bromoacetate → HCID 14101257, compound

https://huagongshe.com/reaction/333100

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
Reactant3-Amino-1-propanolHCID 9086—
SolventWaterHCID 962—
ProductHCID 14101257HCID 1410125763%

Reaction Conditions

Temperature7.5 °C

Reaction Steps

3-Aminopropan-1-ol (154 g; 2.05 mol) is cooled to −5° C. Ethyl bromoacetate (143.6 g: 817 mmol) is added dropwise over a period of 1.5 hours maintaining the temperature around 5-10° C. The stirring is continued for 10 minutes. LC-MS showed that all ethyl bromoactetate has reacted. Then water (570 ml) is added to the reaction mixture. The aqueous mixture is washed three times with ethylacetate (3 times 140 ml). The combined organic phases are back extracted with water (2 times 140 ml). The aqueous phases are combined and saturated with sodium chloride (255 g). The aqueous solution is extracted with methylene chloride (6 times 750 ml). The combined organic phases are dried over sodium sulfate and the solvent is removed under reduced pressure. A yellow oil is obtained (83 g; yield 63%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877961B2
Source datasetuspto-grants-2014_11
ORD IDord-a2b0a9c4530d4726862a97db3b834e54
Source noteuspto-grants-2014_11