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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1740078Generated: November 2, 2026

Ethyl bromoacetate → 1-Boc-4-ethoxycarbonylmethoxypiperidine

https://huagongshe.com/reaction/1740078

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantTert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
SolventTetrahydrofuranHCID 8028—
Product1-Boc-4-ethoxycarbonylmethoxypiperidineHCID 1051739143.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 10.05 g of 1-t-butoxycarbonyl-4-hydroxypiperidine and 50 ml of tetrahydrofuran was stirred with 2.6 g of sodium hydride at room temperature for 30 minutes and then cooled to 0° C. A liquid mixture of 10.02 g of ethyl bromoacetate and 50 ml of tetrahydrofuran was added, and the reaction solution was stirred for 13.5 hours. After addition of saturated ammonium chloride, the reaction solution was extracted with chloroform. The extract was dried over anhydrous sodium sulfate, the insolubles were filtered off, and the solvent was removed by evaporation. The resulting residue was purified by silica gel column chromatography (eluent: ethyl acetate/normal hexane=1:3→1:1) to give 6.28 g of the title compound as a pale yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05968967
Source datasetuspto-grants-1999_10
ORD IDord-b0adc8e8cc184428b6cbe83edfd58aaa
Source noteuspto-grants-1999_10