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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21980Generated: October 26, 2026

Methanol → 3-t-Butoxycarbonylmethyl-10-hydroxymethyl-2-oxo-1-azacyclodecane

https://huagongshe.com/reaction/21980

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium borohydrideHCID 4311764—
ReactantEthyl 3-t-butoxycarbonylmethyl-2-oxo-1-azacyclodecane-10-carboxylateHCID 19930811—
Solventtert-ButanolHCID 6386—
Product3-t-Butoxycarbonylmethyl-10-hydroxymethyl-2-oxo-1-azacyclodecaneHCID 19930843—

Reaction Conditions

Temperature55 °C

Reaction Steps

The major isomer of ethyl 3-t-butoxycarbonylmethyl-2-oxo-1-azacyclodecane-10-carboxylate (0.68 g, 2.0 mmol) is dissolved in t-butanol (10 mL). Sodium borohydride (0.23 g, 6.0 mmol) is added and the reaction is warmed to 55° C. Methanol (2.0 mL) is added over a twenty minute period, and the reaction is kept at 55° C. for an additional 1 hour. The reaction is then partitioned between ethyl acetate and water, and the aqueous phase is extracted several times with ethyl acetate. The combined organic layers are dried (MgSO4), and the solvent is evaporated. The crude product is purified by silica gel chromatography (50% ethyl acetate/hexane) to give 3-t-butoxycarbonylmethyl-10-hydroxymethyl-2-oxo-1-azacyclodecane, MS: M+1=300.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05426103
Source datasetuspto-grants-1995_06
ORD IDord-5fdd0e3dd94345ac930309f298b22ccd
Source noteuspto-grants-1995_06