HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → alpha-(4-Bromophenyl)-3-(tert-butyldimethylsilyloxy)benzyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | alpha-(4-Bromophenyl)-3-(tert-butyldimethylsilyloxy)benzyl alcohol | HCID 53744634 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | alpha-(4-Bromophenyl)-3-(tert-butyldimethylsilyloxy)benzyl chloride | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05658908 |
| Source dataset | uspto-grants-1997_08 |
| ORD ID | ord-b88861a340e24fd58e3fbf2fbaf6169f |
| Source note | uspto-grants-1997_08 |