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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2427932Generated: November 2, 2026

Thionyl Chloride → 4-Phenylbenzoyl chloride

https://huagongshe.com/reaction/2427932

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant(1,1'-Biphenyl)-4-carboxylic acidHCID 66724—
CatalystDimethylformamideHCID 6228—
Product4-Phenylbenzoyl chlorideHCID 84151100%

Reaction Steps

(1,1′-biphenyl)-4-carboxylic acid (20 g, 100.9 mmol) was refluxed for one night in 100 ml of SOCl2 in the presence of a few drops of DMF. Thionyl chloride was removed at ordinary pressure and the residue was triturated in Et2O and filtered. Yield 100% of (1,1′-biphenyl)-4-carbonyl chloride (21.9 g), white crystalline solid. m.p. 116-119° C. 1H-NMR(CHCl3) 7.41-7.73 (7H, m), 8.18 (2H, d, J=8.3 Hz). 13C-NMR(CHCl3) 128.0, 128.1, 129.5, 129.7, 132.4, 132.6, 139.6, 148.7, 168.6

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968748B2
Source datasetuspto-grants-2011_06
ORD IDord-a34f74a6160947e5bfc55b506bb06753
Source noteuspto-grants-2011_06