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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1899754Generated: October 30, 2026

Benzophenone → Benzenemethanol, .alpha.-methyl-.alpha.-phenyl-

https://huagongshe.com/reaction/1899754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzophenoneHCID 3102—
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium ChlorideHCID 25517—
ProductBenzenemethanol, .alpha.-methyl-.alpha.-phenyl-HCID 69031—

Reaction Steps

To this reaction mixture was added dropwise a liquid mixture of 182.22 g (1.1 mol) of benzophenone (3a; R1,R2 =H) and 364 ml of dry THF at 35° to 40° C. over a period of 30 minutes. This mixture was stirred first at that temperature for 2 hours and then at that temperature for 13 hours to complete the reaction. The resulting solution was added to 1,400 g of cooled 10% aqueous ammonium chloride solution with cooling with ice. The mixture was stirred for 30 minutes, allowed to stand, and then subjected to liquid separation, followed by washing with aqueous common salt solution, drying with magnesium sulfate, and concentration to obtain 200.23 g of crude 1,1-diphenylethanol (theoretical yield based on the benzophenone, 98.6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05573878
Source datasetuspto-grants-1996_11
ORD IDord-15f860f9fd944bbdacdc1b61327ec37e
Source noteuspto-grants-1996_11