HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1955804Generated: October 29, 2026
Dimethylformamide → 4-(Cyanomethyl)benzoyl chloride
https://huagongshe.com/reaction/1955804
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 4-(Cyanomethyl)benzoic acid | HCID 270871 | — |
| Product | 4-(Cyanomethyl)benzoyl chloride | HCID 12803948 | — |
Reaction Steps
A solution of 4-cyanomethylbenzoic acid (10.0 g, 62.2 mmol) in thionyl chloride (65 mL) containing DMF (1 mL) was refluxed for three hours, cooled, concentrated, dissolved in hot EtOAc, treated with activated charcoal, filtered through Celite, and concentrated to yield 4-cyanomethylbenzoyl chloride. 4-Cyanomethylbenzoyl chloride was converted to the title compound following the procedure described in step A of Example 82 with the following modifications: 1) 1-(4-cyanomethylphenyl)-2-phenylethanone was chromatographed on silica gel using 2:3 EtOAc/hexane; 2) purification of N-[1-(4-cyanomethylphenyl)-2-phenylethyl]formamide entailed treatment with activated charcoal in EtOAc followed by recrystallization from EtOAc/hexane; and 3) the title compound was chromatographed on silica gel eluting with 10% acetone/EtOAc.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05776983 |
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| Source dataset | uspto-grants-1998_07 |
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| ORD ID | ord-40435f3fb1c246db8964f0b3ad205001 |
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| Source note | uspto-grants-1998_07 |
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