HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1255713Generated: October 28, 2026
Ammonium Hydroxide → 4,6-Dichloronicotinamide
https://huagongshe.com/reaction/1255713
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 4,6-Dichloronicotinic acid | HCID 817158 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4,6-Dichloronicotinamide | HCID 600044 | 95.6% |
Reaction Steps
Oxalyl chloride (7.70 mL, 88.3 mmol) was added over 1 hour to a suspension of 4,6-dichloronicotinic acid (8.47 g, 44.1 mmol) in dimethylformamide (200 mL) at room temperature. The reaction mixture was stirred for an additional 3 hours at room temperature then concentrated in vacuo. The residue was dissolved in CH2Cl2 (200 mL) followed by the dropwise addition of NH4OH (8.3 mL, 130 mmol) over 30 minutes [Note: reaction is exothermic upon addition of NH4OH and care was taken to control the rate of addition so that the reaction temperature did not exceed 25° C.]. The reaction mixture was stirred for an additional 1 hour at room temperature then diluted with water (600 mL) and extracted with EtOAc (4×600 mL). The organic extracts were combined, dried over Na2SO4, filtered and concentrated to give the title compound as a light brown solid (8.05 g, 95% yield). This material was carried forward without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08461135B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-e0ab08f637f547a798a5ce80e0634161 |
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| Source note | uspto-grants-2013_06 |
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