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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1513325Generated: November 5, 2026

Bromide ion → Pseudourea, 2-(p-nitrobenzyl)-2-thio-, monohydrobromide

https://huagongshe.com/reaction/1513325

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromide ionHCID 259—
Reactant4-Nitrobenzyl bromideHCID 66011—
ReactantThioureaHCID 2723790—
SolventAcetoneHCID 180—
ProductPseudourea, 2-(p-nitrobenzyl)-2-thio-, monohydrobromideHCID 11635094.1%

Reaction Steps

Thiourea (8c) (1.55 kg) and acetone (30 L) were added to a 72-L reactor under a nitrogen atmosphere. The mixture was agitated. 4-nitrophenylmethyl bromide (8d) (4.00 kg) and acetone (15 L) were added to a separate flask. The mixture was stirred until the bromide dissolved (warming may be required). The solution of the bromide was added to the mixture of thiourea, keeping the temperature below 40° C. A thick solution formed within 30 minutes. After stiffing for 2 h, HPLC analysis of the mixture shows >99% conversion. The mixture was filtered, and the filter cake was rinsed with a 1:1 MTBE: acetone solution (8 L). The solids were dried to give 5.09 kg (93% yield) of the desired product (8a) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08217172B2
Source datasetuspto-grants-2012_07
ORD IDord-a2ddd57e1f59443f9dfb1d9db5f8f946
Source noteuspto-grants-2012_07