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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1670826Generated: October 31, 2026

Water → Methyl 2-(4-hydroxypiperidin-1-yl)acetate

https://huagongshe.com/reaction/1670826

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantMethyl bromoacetateHCID 60984—
ReactantPiperidin-4-olHCID 79341—
SolventDichloromethaneHCID 6344—
ProductMethyl 2-(4-hydroxypiperidin-1-yl)acetateHCID 2883775361.2%

Reaction Steps

Treat a 0° C. solution of 4-hydroxy-piperidine (20.0 g, 0.19 mol) and (CH3CH2)3N (24.0 g, 0.24 mol) in CH2Cl2 (200 mL) with methyl bromoacetate (30.21 g, 0.197 mol), warm to room temperature, and stir 2 hours at room temperature under N2. Dilute the reaction with water and extract with 3:1 chloroform:isopropanol. Dry the organic layer (Na2SO4), remove the solvent in vacuo to afford crude product, and purify with a 5% methanol in CH2Cl2 to afford 20.13 g (59%) of the titled product. Rf=0.13 (9/1 CH2Cl2/methanol). ES MS (m/z): 174 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994176B2
Source datasetuspto-grants-2011_08
ORD IDord-6feb880458f54c73aec6f5c111342c02
Source noteuspto-grants-2011_08