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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 428055Generated: October 31, 2026

HCID 18357646, compound → HCID 18357488, compound

https://huagongshe.com/reaction/428055

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 18357646HCID 18357646—
ReactantHCID 178455850HCID 178455850—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18357488HCID 18357488—

Reaction Steps

To a stirred solution of 2 g of 2-[2-(1,2-benzisoxazol-3-yl)-phenyl]acetaldehyde in 50 ml of tetrahydrofuran at −78° C. under a nitrogen atmosphere was added 10 ml of a 1 M solution of allyl magnesium bromide in diethyl ether. The solution was warmed to room temperature and stirred for a further 2 h then quenched by addition of 50 ml of saturated aqueous ammonium chloride. The aqueous layer was extracted with 150 ml then 100 ml of dichloromethane and the combined organic extracts dried over sodium sulfate and evaporated to give crude product which was purified by chromatography eluting with 20% ethyl acetate in hexane, affording 1 g of 3-[2-(2-Hydroxy-4-pentenyl)phenyl]-1,2-benzisoxazole, 1H-NMR (200 MHz, CDCl3) d 5.8 (CH═CH2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313139B1
Source datasetuspto-grants-2001_11
ORD IDord-677e87a08c84471ea35ddd7c72c4bfe1
Source noteuspto-grants-2001_11