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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018927Generated: October 31, 2026

Allyl bromide → HCID 12052162, compound

https://huagongshe.com/reaction/1018927

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 178527942HCID 178527942—
SolventEthanolHCID 702—
ProductHCID 12052162HCID 12052162—

Reaction Steps

To a suspension of 4-phenylphthalazine-1-thiol (Example 1B) (238 mg, 1 mmol) in ethanol (40 ml) is added aqueous KOH (1 molar, 1 ml). After 10 minutes, allylbromide (0.1 ml, 1 mmol) is added, and the mixture is stirred at room temperature for 4 days. After the solvent is evaporated, the residue is extracted with CH2Cl2. The organic phase is evaporated and the residue is stirred with isopropyl ether. Filtration gives the pure title compound, which is recrystallized from ethanol (130 mg). (R1=vinyl, R2=phenyl, A=benzene, Y1=CH2, m=0, n=1, p=0, q=0).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06486158B1
Source datasetuspto-grants-2002_11
ORD IDord-718d2d85db4e464985e7e7c6366a2e76
Source noteuspto-grants-2002_11