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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19951Generated: October 29, 2026

Thionyl Chloride → HCID 21976878, compound

https://huagongshe.com/reaction/19951

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant3-Bromo4-(N,N-dimethylsulfamoyl)benzyl alcoholHCID 65751018—
SolventDichloromethaneHCID 6344—
SolventHexaneHCID 8058—
ProductHCID 21976878HCID 2197687899.4%

Reaction Steps

To a solution of OBS02002 (5.0 g, 16.12 mmol) in anhydrous DCM (50 mL) was added thionyl chloride (1.76 mL, 24.18 mmol). The mixture was stirred at room temperature for 2 h and the volatiles removed in vacuo. The residue was re-dissolved and co-evaporated three times with DCM (3×20 mL) to give a yellow oil which solidified on standing. The solid was stirred in n-hexane, filtered and air-dried to give OBS02003 as an off-white solid (5.01 g, 95%). TLC [SiO2, EtOAc-n-hexane (1:1)] Rf=0.79; 1H-NMR (270 MHz, CDCl3)=3.05 (6H, s), 4.51 (2H, s), 7.32 (1H, dd, J=2.2, 8.4), 7.48 (1H, d, J=8.4), 7.62 (1H, d, J=2.2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745472B2
Source datasetuspto-grants-2010_06
ORD IDord-2fbbf35ada3b43daa1f8ca01bf5c081f
Source noteuspto-grants-2010_06