HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 4-Phenylbenzoyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | (1,1'-Biphenyl)-4-carboxylic acid | HCID 66724 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Product | 4-Phenylbenzoyl chloride | HCID 84151 | 100% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07968748B2 |
| Source dataset | uspto-grants-2011_06 |
| ORD ID | ord-a34f74a6160947e5bfc55b506bb06753 |
| Source note | uspto-grants-2011_06 |