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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158203Generated: October 25, 2026

Water → (3-Methoxyphenyl)(2-(2,4,6-trimethoxybenzylthio)phenyl)methanol

https://huagongshe.com/reaction/1158203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3-MethoxybenzaldehydeHCID 11569—
Reactant(2-Bromophenyl)(2,4,6-trimethoxybenzyl)sulfaneHCID 66870845—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventEthyl acetate hexaneHCID 21226206—
Product(3-Methoxyphenyl)(2-(2,4,6-trimethoxybenzylthio)phenyl)methanolHCID 6864365270%

Reaction Steps

To a solution of 0.35 g (2-bromophenyl)(2,4,6-trimethoxybenzyl)sulfane (0.96 mmol) in dry THF was added slowly 1.2 eq n-BuLi. The reaction was stirred 25 minutes at −78° C. before 1.2 eq 3-methoxybenzaldehyde was added slowly. The reaction was warmed to ambient temperature and stirred for one additional hour before the addition of water. The mixture was extracted with ethyl acetate. The combined organic extracts were washed with brine, dried over magnesium sulfate, filtered and concentrated. Flash silica chromatography (hexane:ethyl acetate 80:20) afforded 0.288 g product (0.68 mmol, 70% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807713B2
Source datasetuspto-grants-2010_10
ORD IDord-e9e4de51aafc4a4f99f02489027f754c
Source noteuspto-grants-2010_10