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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 273818Generated: November 1, 2026

Benzophenone → HCID 11020538, compound

https://huagongshe.com/reaction/273818

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzophenoneHCID 3102—
ReactantHCID 178418473HCID 178418473—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11020538HCID 11020538—

Reaction Steps

To 29 g of benzophenone in 150 mL of tetrahydrofuran (THF) at 0° C. was added 88 mL of 2M allyl magnesium chloride. After 16 hrs, the starting material was completely consumed as indicated by thin layer chromatography (TLC). To the reaction mixture was added 1 mL of methanol to quench the excess Grinard reagent. The THF was distilled in vacuo and the residue was shaken with dilute aqueous hydrochloric acid and chloroform. The layers were separated and the aqueous phase was extracted with chloroform. The combined organic layers were dried with sodium sulfate and concentrated to give 37 g of 1,1-diphenyl-3-buten-1-ol which is characterized by:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05387617
Source datasetuspto-grants-1995_02
ORD IDord-921fc5fea47c4b0d8db844851950cdc7
Source noteuspto-grants-1995_02