Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767177Generated: November 2, 2026

Methanol → HCID 11064222, compound

https://huagongshe.com/reaction/1767177

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. Ti(IV)isopropoxide (12.5 g, 0.044 mol) was added and stirred for 30 min. at room temperature. After cooling the reaction mixture to −50° C. to −55° C., sodium borohydride (1.67 g, 0.044 mol) was added in 4 portions maintaining the temperature between −50° C. and −55° 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 saturated ammonium chloride solution (2×50 mL), water (50 mL) and brine solution (50 mL), and concentrated to obtain the title compound. Yield: 7.5 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07232920B2
Source datasetuspto-grants-2007_06
ORD IDord-143c9f6f71d34abc8e87416d1bc0bf23
Source noteuspto-grants-2007_06