HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2184350Generated: November 1, 2026
Ammonia → 3-{4-[(3-Fluorophenyl)methoxy]phenyl}-2-methylprop-2-enamide
https://huagongshe.com/reaction/2184350
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 3-{4-[(3-Fluorophenyl)methoxy]phenyl}-2-methylprop-2-enoic acid | HCID 69289494 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-{4-[(3-Fluorophenyl)methoxy]phenyl}-2-methylprop-2-enamide | HCID 69289701 | 65% |
Reaction Steps
305 mg (1.07 mmol) of 3-[4-(3-fluoro-benzyloxy)-phenyl]-2-methyl-acrylic acid is dissolved in 8 ml of dichloromethane and one drop of dimethylformamide is added. The solution is cooled to 0° C. and treated dropwise with 676 mg (5.33 mmol) oxalyl chloride. The resulting solution is stirred at 0° C. for additional 30 minutes, then 2 hours at RT. Evaporation of the solvent leaves the crude acid chloride which is dissolved in 5 ml THF. This solution is slowly added under stirring to 10 ml of concentrated ammonia. The precipitate is filtered off and recrystallised from methanol to yield 199 mg (65%) of a colorless solid. MS: m/e=286.2 (M++H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06900354B2 |
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| Source dataset | uspto-grants-2005_05 |
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| ORD ID | ord-6e24374e65344b4b8ecacfa75efd3abc |
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| Source note | uspto-grants-2005_05 |
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