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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2258315Generated: October 26, 2026

Thionyl Chloride → alpha-(4-Bromophenyl)-3-(tert-butyldimethylsilyloxy)benzyl chloride

https://huagongshe.com/reaction/2258315

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactantalpha-(4-Bromophenyl)-3-(tert-butyldimethylsilyloxy)benzyl alcoholHCID 53744634—
SolventDichloromethaneHCID 6344—
Productalpha-(4-Bromophenyl)-3-(tert-butyldimethylsilyloxy)benzyl chlorideHCID 22350043—

Reaction Steps

The crude benzhydryl alcohol (53.2 g, 135 mmol) was dissolved in 1000 mL of dichloromethane and 14.7 mL (202 mmol) of thionyl chloride was added dropwise. The solution was stirred overnight at room temperature and the solvent was removed under vacuum. The crude product was redissolved in 500 mL of toluene and the solvent again was removed under vacuum to eliminate excess thionyl chloride, providing crude α-(4-bromophenyl)-3-(tert-butyldimethylsilyoxy) benzyl chloride as a dark oil. NMR (200 MHz, CDCl3): δ0.2 (s,6H); 1.0 (s,9H); 6.0 (s,1H); 6.78 (dd,J1 =1 Hz,J2 =8 Hz,1H); 6.9 (m,2H); 7.2 (t,J=8 Hz,2H); 7.27 and 7.47 (AB q,J=8 Hz,4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05658908
Source datasetuspto-grants-1997_08
ORD IDord-b88861a340e24fd58e3fbf2fbaf6169f
Source noteuspto-grants-1997_08