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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582265Generated: October 27, 2026

Benzyl Bromide → S-benzylthiobenzimidate hydrobromide

https://huagongshe.com/reaction/1582265

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantThiobenzamideHCID 683563—
SolventDichloromethaneHCID 6344—
ProductS-benzylthiobenzimidate hydrobromideHCID 1262465485%

Reaction Steps

To a solution of thiobenzamide (0.307 g, 2.24 mmol) in CH2Cl2 (11 mL) was added benzyl bromide (0.26 mL, 2.19 mmol) and the resultant solution was heated to reflux for 2 h. The mixture was cooled to room temperature and concentrated under reduced pressure. The resultant yellow solid was dried under vacuum to provide S-benzylthiobenzimidate hydrobromide (0.573 g, 85%). 1H NMR (DMSO-d6) δ4.76 (s, 2H), 7.34-7.44 (m, 3H), 7.51-7.54 (m, 2H), 7.61-7.66 (m, 2H), 7.78-7.83 (m, 1H), 7.88-7.91 (m, 2H), 11.92 (br s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06734191B2
Source datasetuspto-grants-2004_05
ORD IDord-6a77445ff1dc452389811ea7b834a800
Source noteuspto-grants-2004_05