HCID 13255323, compound → HCID 21326944, compound

HRID 1439291Notes

Reaction equation

HRID 1439291 reaction equation
[CH2:1]([NH:17][C:18]1[CH:38]=[CH:37][C:21]([C:22]([O:24][CH:25]2[CH2:30][O:29]C(C3C=CC=CC=3)[O:27][CH2:26]2)=[O:23])=[CH:20][CH:19]=1)[CH2:2][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][CH3:16].[H][H]>[Pd].C(O)(=O)C>[CH2:1]([NH:17][C:18]1[CH:19]=[CH:20][C:21]([C:22]([O:24][CH:25]([CH2:26][OH:27])[CH2:30][OH:29])=[O:23])=[CH:37][CH:38]=1)[CH2:2][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][CH3:16]

Participants

5

Procedure

A mixture of 2-phenyl-1,3-dioxan-5-yl 4-(n-hexadecylamino)benzoate, palladium black, and acetic acid is shaken under one atmosphere of hydrogen until hydrogen uptake ceases. The catalyst is separated by filtration and the solvent is evaporated. Crystallization from acetonitrile affords 1,3-dihydroxy-2-propyl 4-(n-hexadecylamino)benzoate as a white solid.

Workup

  1. customThe catalyst is separated by filtration
  2. customthe solvent is evaporated
  3. customCrystallization from acetonitrile

Sources & evidence

ORD record
ord-f5d659f5c83545b2812a2fda35d14e45
Source dataset
uspto-grants-1977_11
Patent number
US04058550

Reaction notes

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