HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2163776Generated: October 31, 2026
Pyridine → 2,3-Dihydroxypropyl-4-hexadecylaminobenzamide
https://huagongshe.com/reaction/2163776
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 3-Amino-1,2-propanediol | HCID 73561 | — |
| Reactant | HCID 70506019 | HCID 70506019 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 2,3-Dihydroxypropyl-4-hexadecylaminobenzamide | HCID 20437388 | — |
Reaction Steps
A slurry of 8.0 g. of 4-(hexadecylamino)benzoic acid hydrochloride in 175 ml. of CH2Cl2 and 50 ml. of glyme containing 10 ml. of thionyl chloride was heated at reflux for 2 hours. The clear solution was concentrated in vacuo giving 9.5 g. of an amber oil. This oil was diluted with 50 ml. of pyridine containing 0.1 g. of 4-dimethylaminopyridine and 9.1 g. of 3-amino-1,2-propandiol. The reaction was stirred for two days at room temperature. The solution was partitioned between ether and water. The water phase was extracted twice more with 100 ml. of chloroform and ether. The combined organic layer was extracted with water, dried over MgSO4 and evaporated to a tacky solid. The solid was recrystallized from acetone-water and a second time from benzene. A small sample was recrystallized from acetonitrile, m.p. 121°-122° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04136256 |
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| Source dataset | uspto-grants-1979_01 |
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| ORD ID | ord-e56e52f8e439426ca5dc7ce3590f707e |
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| Source note | uspto-grants-1979_01 |
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