HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 976284Generated: October 29, 2026
Oxalyl chloride → 4'-(Benzyloxy)[1,1'-biphenyl]-4-carbaldehyde
https://huagongshe.com/reaction/976284
Participants
| Role | Name | HCID | Charge |
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| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 4'-(Benzyloxy)[1,1'-biphenyl]-4-carboxylic acid | HCID 14744793 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4'-(Benzyloxy)[1,1'-biphenyl]-4-carbaldehyde | HCID 20099902 | 41% |
Reaction Steps
Oxalyl chloride (1.72 ml) and dry dimethylformamide (2 drops) were added to a stirred suspension of 4'-benzyloxy-4-biphenylcarboxylic acid (3.04 g) in dry dichloromethane (100 ml). The reaction mixture was stirred for 12 hours at ambient temperature. The mixture was evaporated to dryness. Triphenylphosphine (5.2 g) and bis(triphenylphosphine) copper [I] tetrahydroborate (6.0 g) was added to a solution of the crude product in acetone (150 ml). The mixture was stirred at ambient temperature for 2 hours. The mixture was filtered and the filtrate evaporated. The residue was purified by medium pressure chromatography on silica gel using a mixture of 20% dichloromethane/hexane to remove less polar impurities, followed by ethyl acetate as eluant to give 4'-benzyloxy-4-biphenylcarboxaldehyde as a colourless solid (41% yield), m.p. 122°-123° C., NMR (CDCl3): 5.1 (2H, s), 7.1 (2H, d), 7.4-7.6 (7H, m), 7.7-7.9 (4H, d of d), and 10.0 (1H, s); m/z 289 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05612352 |
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| Source dataset | uspto-grants-1997_03 |
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| ORD ID | ord-6519661ef82f4e16b540033dbd813c4d |
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| Source note | uspto-grants-1997_03 |
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