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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 857178Generated: October 26, 2026

Water → 4-[1-(3,4-Dimethoxyphenoxy)-4-hydroxybutyl]benzonitrile

https://huagongshe.com/reaction/857178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant(Dimethyl sulfide)trihydroboronHCID 12423031—
Reactant4-[1-(3,4-Dimethoxyphenoxy)-3-butenyl]benzonitrileHCID 21867689—
ReactantSodium;3-oxidodioxaborirane;tetrahydrateHCID 23693097—
SolventTetrahydrofuranHCID 8028—
Product4-[1-(3,4-Dimethoxyphenoxy)-4-hydroxybutyl]benzonitrileHCID 2186772678%

Reaction Steps

Borane-methyl sulfide complex (2 M in ether, 11 mL, 22 mmol) was added dropwise to a cooled (−5° C.) solution of 4-[1-(3,4-dimethoxy-phenoxy)-3-butenyl]benzonitrile (from step (a) above; 17.6 g, 56.8 mmol) in dry THF (15 mL) over a period of 15 minutes (during which time the reaction temperature rose to 0° C.). The resulting mixture was stirred at between 0 and 10° C. for 1.5 h, before being allowed to warm to rt. Stirring was continued for a further 3.5 h at this temperature before water (22 mL) and sodium perborate tetrahydrate (11 g, 66 mmol) were added. The biphasic mixture was stirred for 2 h at rt before the water layer was separated and extracted with ether. The combined organic layers were washed with brine, dried and concentrated in vacuo. The resulting residue was purified by chromatography on silica gel, eluting with IPA:ethyl acetate:heptane (5:25:76) to yield 14.5 g (77%) of the sub-title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07144914B2
Source datasetuspto-grants-2006_12
ORD IDord-f3baa0c99e484c268d4e0acaa82bf1ae
Source noteuspto-grants-2006_12