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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904811Generated: November 2, 2026

Methanol → Ethyl 4-hydroxypiperidine-1-carboxylate

https://huagongshe.com/reaction/1904811

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantAmmonium ChlorideHCID 25517—
ReactantEthyl 4-oxo-1-piperidinecarboxylateHCID 34767—
ReactantSodium borohydrideHCID 4311764—
SolventWaterHCID 962—
ProductEthyl 4-hydroxypiperidine-1-carboxylateHCID 96394—

Reaction Steps

To a suspension of 68.5 parts of ethyl 4-oxo-1-piperidinecarboxylate in 240 parts of methanol was added portionwise 3.8 parts of sodium borohydride at a temperature between 20°-30° C. (the reaction mixture was cooled if necessary in a water-bath). After the addition was complete, the whole was stirred for 30 minutes. The reaction mixture was then poured into a mixture of 53.5 parts of ammonium chloride and 400 parts of water. The methanol was evaporated. The product was extracted with trichloromethane. The extract was dried and evaporated. The oily residue was distilled in vacuo, yielding 60 parts of oily ethyl 4-hydroxy-1-piperidinecarboxylate; bp. 140° C. at 1.4 mm. pressure; nD20 : 1.4796; d2020 : 1.1166 (3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04839374
Source datasetuspto-grants-1989_06
ORD IDord-23412feb2b8e497ab6c1a34cc32e8742
Source noteuspto-grants-1989_06