HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701397Generated: October 26, 2026
Benzyl Alcohol → Benzyl (5-n-butyl-2-pyridyl)carbamate
https://huagongshe.com/reaction/1701397
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Fusaric Acid | HCID 3442 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Benzyl (5-n-butyl-2-pyridyl)carbamate | HCID 53891397 | 57.4% |
Reaction Steps
Diphenylphosphoryl azide (1.5 g., 5.58 mmoles) was added to a solution of 5-n-butylpyridine-2-carboxylic acid (1.0 g., 5.58 mmoles), triethylamine (0.565 g., 5.58 mmoles), and benzyl alcohol (0.663 g., 6.12 mmoles) in 1,4-dioxane (9.0 ml.) at 25°. The stirred solution was heated until an exothermic reaction began. When the exothermic reaction had subsided, the solution was heated under reflux for 1.5 hours. The reaction mixture was concentrated and the residue dissolved in toluene. This solution was washed successively with water, 10% aqueous sodium bicarbonate, and brine, and then dried over sodium sulfate. The solution was concentrated and the residue recrystallized from 2-propanol to give the title compound (0.91 g., 57%), m.p. 142°-143°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04192944 |
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| Source dataset | uspto-grants-1980_03 |
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| ORD ID | ord-21efb01674584598a1be13e737e3f420 |
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| Source note | uspto-grants-1980_03 |
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