HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5011Generated: October 25, 2026
Nicotinic Acid → Nicotinoyl chloride
https://huagongshe.com/reaction/5011
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nicotinic Acid | HCID 938 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 4-(4-Tert-butylphenoxy)butan-1-OL | HCID 13313737 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Nicotinoyl chloride | HCID 82604 | — |
Reaction Steps
Nicotinoyl chloride was prepared by treating 100 g (0.81 mole) of nicotinic acid with 280 ml of thionyl chloride at reflux for two hours. The excess thionyl chloride was removed in vacuo and the crystalline acid chloride hydrochloride was suspended in 500 ml of dichloromethane. To the stirred mixture was added 66 g (0.30 mole) of 4-p-t-butylphenoxy-1-butanol dissolved in 400 ml of dichloromethane. After forty-eight hours the mixture was washed with one liter of saturated sodium bicarbonate. The dichloromethane solution was dried over magnesium sulfate and evaporated to a syrupy residue. The material was chromatographed on 1 kg of silica gel with elution by dichloromethane-methanol, 96:4, to afford 43.8 g (45%) of the nicotinate ester as an oil. The hydrobromide salt was prepared by treatment of a solution of 43.8 g in 800 ml of ethyl acetate with 30 ml of 4.5N hydrogen bromide in ether. The precipitate was collected, washed with pentane and dried, m.p. 132°-133° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05242936 |
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| Source dataset | uspto-grants-1993_09 |
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| ORD ID | ord-d238f04b14bc48fe99e1c99449a0250c |
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| Source note | uspto-grants-1993_09 |
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