Water → HCID 21326952, compound

HRID 615062Notes

Reaction equation

HRID 615062 reaction equation
Cl.[CH2:2]([NH:18][C:19]1[CH:27]=[CH:26][C:22]([C:23](Cl)=[O:24])=[CH:21][CH:20]=1)[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH3:17].O[CH:29]([OH:33])[C:30](=[O:32])[CH3:31].C(Cl)(Cl)Cl.[OH2:38]>CN(C)C1C=CN=CC=1>[CH2:2]([NH:18][C:19]1[CH:27]=[CH:26][C:22]([C:23]([O:38][CH2:31][C:30]([CH2:29][OH:33])=[O:32])=[O:24])=[CH:21][CH:20]=1)[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH3:17]

Participants

6

Procedure

The compound 4-(n-hexadecylamino)benzoyl chloride hydrochloride (4.16 g.) is added to a mixture of 3.6 g. of dihydroxyacetone and 2.44 g. of 4-dimethylaminopyridine in an ice bath. After 4 hours at room temperature, the mixture is treated with chloroform and water. The chloroform extract is chromatographed rapidly and evaporated in vacuo to yield 3-hydroxyacetonyl 4-(n-hexadecylamino)benzoate.

Workup

  1. extractionThe chloroform extract
  2. customis chromatographed rapidly
  3. customevaporated in vacuo

Sources & evidence

ORD record
ord-5e77183b24054f38b47e1a8215fa160a
Source dataset
uspto-grants-1979_03
Patent number
US04146546

Reaction notes

Loading…