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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2279485Generated: October 30, 2026

Hydrochloric Acid → (αS)-3,4-Dichloro-α-ethylbenzenemethanol

https://huagongshe.com/reaction/2279485

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethylaniline-boraneHCID 83312—
Reactant1-(3,4-Dichlorophenyl)-1-propanoneHCID 599598—
Reactant(R)-2-Methyl-CBS-oxazaborolidineHCID 9838490—
SolventMethanolHCID 887—
Solventtert-Butyl methyl etherHCID 15413—
Product(αS)-3,4-Dichloro-α-ethylbenzenemethanolHCID 2566579467%

Reaction Conditions

Temperature40 °C

Reaction Steps

A 250 mL round-bottom flask was charged with MTBE (35 mL), a solution of (R)-1-methyl-3,3-diphenylhexahydropyrrolo[1,2-c][1,3,2]oxazaborole (2.51 mL, 2.51 mmol) and borane diethylaniline (4.45 mL, 25.1 mmol) at RT then heated to 40° C. A MTBE (20 mL) solution of 156 (6.00 g, 25.1 mmol) was added dropwise and the reaction was stirred at 40° C. for 3 h. The reaction was cooled to RT and MeOH (5 mL) was then added slowly, followed by 1M HCl and the reaction was stirred for 18 h. The water was removed and the remaining organic phase dried (Na2SO4), filtered and concentrated to get a light gray oil. The crude product was purified by SiO2 chromatography (SNAP 100) eluting with EtOAc/hexane (1:3) to afford 3.45 g (66%) of (S)-1-(3,4-dichlorophenyl)propan-1-ol (158) as a clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133187B2
Source datasetuspto-grants-2015_09
ORD IDord-67d66dd55314418ca516d09110611aff
Source noteuspto-grants-2015_09