HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 584378Generated: October 30, 2026
Dimethylformamide → HCID 22344577, compound
https://huagongshe.com/reaction/584378
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | delta-Benzoylvaleric acid | HCID 223595 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22344577 | HCID 22344577 | 89% |
Reaction Steps
Oxalyl chloride (0.508 ml) and N,N-dimethylformamide (catalytic amount) were added to a solution of 6-oxo-6-phenylhexanoic acid (1.00 g) in tetrahydrofuran (15 ml) at room temperature, which was stirred at room temperature for 1 hour and concentrated. The residue was dissolved in ethyl acetate (25 ml) and added dropwise to a stirred mixture of 25% aqueous ammonia (20 ml) and ethyl acetate (25 ml) at 0° C. After stirring at room temperature for 2 hours water (200 ml) was added and extracted with ethyl acetate. The ethyl acetate layer was washed with an aqueous saturated solution of sodium chloride, dried (MgSO4) and concentrated. The remaining crystals were recrystallized from ethyl acetate-hexane to obtain 6-oxo-6-phenylhexanamide (885 mg, yield 89%) as colorless crystals. m.p. 113-114° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06924300B2 |
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| Source dataset | uspto-grants-2005_08 |
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| ORD ID | ord-ae82935aadf647dfb53f799d4d7b2acd |
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| Source note | uspto-grants-2005_08 |
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