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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1733366Generated: October 29, 2026

Allyl bromide → HCID 178460856, compound

https://huagongshe.com/reaction/1733366

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 131711976HCID 131711976—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
ProductHCID 178460856HCID 178460856—

Reaction Steps

To a suspension of 1-iminophenylmethyl-2-(3-carbomethoxythioureido)-4-propylthiobenzene (1.0 g.) in acetone (30 ml.) and water (10 ml.) there is added aqueous sodium hydroxide (0.21 g.). The mixture is stirred at room temperature for one hour (a solution forms 20 minutes after the addition of sodium hydroxide) and to it there is added allyl bromide (0.36 g.). The solution is stirred at room temperature for two hours and is then poured into water (300 ml.). The mixture is stirred at room temperature for 24 hours and is vacuum filtered. The tacky yellow solid is stirred in hexane (50 ml.) and is filtered to yield 0.35 g. of 1-iminohexylmethyl-2-(3-carbomethoxy-S-isothioureido)-4-propylthiobenzene, m.p. 70°-72° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04241079
Source datasetuspto-grants-1980_12
ORD IDord-906bdb8ecd384d859145044b2e6230f5
Source noteuspto-grants-1980_12