HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 414590Generated: October 31, 2026
Phenylacetyl chloride → HCID 19774552, compound
https://huagongshe.com/reaction/414590
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenylacetyl chloride | HCID 7679 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 10797035 | HCID 10797035 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 19774552 | HCID 19774552 | 84.6% |
Reaction Steps
To a solution of N-(1H-pyrrol-1-yl)-4-pyridinamine (6 g) in 400 ml of dichloromethane containing sodium bicarbonate (6.3 g) was added a solution of phenylacetyl chloride (6.7 g) in 50 ml of dichloromethane. After stirring four hours at ambient temperature, the reaction mixture was evaporated, stirred with water and extracted with ether. The organic extract was washed with water and saturated sodium chloride solution, dried over anhydrous magnesium sulfate, filtered and evaporated to 11 g of an oil. This oil was purified by flash chromatography (silica, 25% ethyl acetate in dichloromethane) to give 10 g of an oil. This oil was converted to the hydrochloride salt in ethanol to give 10.4 g of crystals, d 203°-205°. A 3 g sample was recrystallized from ethanol-ether to give 2.8 g of needles, d 203°-204°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04792562 |
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| Source dataset | uspto-grants-1988_12 |
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| ORD ID | ord-9b59a1f4ba1945df8de5984c086dc818 |
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| Source note | uspto-grants-1988_12 |
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