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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2245776Generated: October 25, 2026

Toluene → 4-(4-Dimethylaminophenylsulfanyl)-2-methylpent-2-en-1-ol

https://huagongshe.com/reaction/2245776

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantDiisobutylaluminumhydrideHCID 21225700—
Reactant4-(4-Dimethylaminophenylsulfanyl)-2-methylpent-2-enoic acid methyl esterHCID 68545878—
SolventTetrahydrofuranHCID 8028—
Product4-(4-Dimethylaminophenylsulfanyl)-2-methylpent-2-en-1-olHCID 6854312188%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4-(4-dimethylaminophenylsulfanyl)-2-methylpent-2-enoic acid methyl ester (0.279 g, 1.0 mmol) in dry THF (4 mL) at 0° C. was added dropwise a solution of di-isobutylaluminium hydride in toluene (1M, 3.0 mL, 3.0 mmol), under an atmosphere of argon. After stirring at 0° C. for one hour (TLC monitoring), the mixture was quenched by addition of methanol (0.5 mL: CAUTION), then water (0.3 mL), 5% aqueous sodium hydroxide solution (0.3 mL) and lastly 30% aqueous sodium potassium tartrate (4 mL). The mixture was stirred for 2 hours at 20° C., then extracted with diethyl ether (3×10 mL). The combined organic layers were dried over anhydrous MgSO4, filtered and evaporated to give the title compound (0.22 g, 88%) as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07683185B2
Source datasetuspto-grants-2010_03
ORD IDord-ec9bfa5c612143cd99f27e6e868d2997
Source noteuspto-grants-2010_03