Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767176Generated: November 1, 2026

Methanol → HCID 11064222, compound

https://huagongshe.com/reaction/1767176

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium borohydrideHCID 4311764—
Reactanttert-Butyl (R)-6-Cyano-5-hydroxy-3-oxohexanoateHCID 9794547—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11064222HCID 11064222—

Reaction Steps

A solution of tert-butyl (5R)-6-cyano-5-hydroxy-3-oxohexanoate (10 g, 0.044 mol) in THF (60 mL) was stirred under nitrogen and methanol (20 mL) was added. The reaction mixture was stirred for 15 min. and cooled to −50° C. to −55° C. CeCl3.7H2O (16.4 g, 0.044 mol) was added and stirred for 30 min., maintaining the temperature between −50 and −55° C. Sodium borohydride (2.5 g, 0.066 mol) was added in 6 portions maintaining the temperature between −70 and −90° C. The resulting mixture was stirred for 1 h at the same temperature. After warming the reaction mixture to RT, it was concentrated to a residue under vacuum at about 45° C. Methanol (60 mL) was added and the resulting mixture was concentrated. The resulting residue was cooled to RT, water (50 mL) was added and the resulting aqueous mixture was extracted with ethyl acetate (100 mL×2). The combined organic layer was washed with brine solution (50 mL), and concentrated to obtain title compound. Yield: 5 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07232920B2
Source datasetuspto-grants-2007_06
ORD IDord-a6109c4e14c349399cbd394cd53d969a
Source noteuspto-grants-2007_06