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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1733364Generated: November 1, 2026

Allyl bromide → HCID 178460855, compound

https://huagongshe.com/reaction/1733364

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 131711970HCID 131711970—
ReactantHCID 178460854HCID 178460854—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
ProductHCID 178460855HCID 178460855—

Reaction Steps

To a suspension of 3-iminophenylmethyl-4-(3-carbomethoxythioureido)benzophenone (2.09 g.; 0.005 mole) in acetone (40 ml.) and water (6.0 ml.) is added an aqueous sodium hydroxide solution (50% aqueous; 0.4 g.). The suspension is stirred at room temperature for one hour and then allyl bromide (0.6 g.; 0.005 mole) is added and the solution is stirred at room temperature over the weekend. The precipitate which forms is collected by filtration and then dried to afford 1.3 g. of 3-iminophenylmethyl)-4-(3-carbomethoxy-S-allylisothioureido)benzophenone, m.p. 125°-127° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04241079
Source datasetuspto-grants-1980_12
ORD IDord-3da3ba2f52664c0da2cb6dbef50b45b0
Source noteuspto-grants-1980_12