p-Toluenesulfonic acid → 3-Hydroxypropyl 3-fluoro-4-(hexadecylamino)benzoate

HRID 1389091Notes

Reaction equation

HRID 1389091 reaction equation
[F:1][C:2]1[CH:3]=[C:4]([CH:9]=[CH:10][C:11]=1[NH:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH3:28])[C:5]([O:7][CH3:8])=[O:6].C(O)[CH2:30][CH2:31][OH:32].C1(C)C=CC(S(O)(=O)=O)=CC=1>>[F:1][C:2]1[CH:3]=[C:4]([CH:9]=[CH:10][C:11]=1[NH:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH3:28])[C:5]([O:7][CH2:8][CH2:30][CH2:31][OH:32])=[O:6]

Participants

4

Reactant 3

HCID 6101p-Toluenesulfonic acidHCID 104421,3-PropanediolHCID 20536536Methyl 3-fluoro-4-(hexadecylamino)benzoate

Product 1

HCID 205364653-Hydroxypropyl 3-fluoro-4-(hexadecylamino)benzoate

Procedure

A mixture of 2.25 g of methyl 3-fluoro-4-(hexadecylamino)benzoate, 280 mg of 1,3-propanediol and 1.37 g. of p-toluenesulfonic acid is heated at 180° C. for 18 hours and then is partitioned between ether and 3% aqueous sodium carbonate solution. The ether layer is separated, dried, and evaporated to yield 3-hydroxypropyl 3-fluoro-4-(hexadecylamino)benzoate.

Workup

  1. customis partitioned between ether and 3% aqueous sodium carbonate solution
  2. customThe ether layer is separated
  3. customdried
  4. customevaporated

Sources & evidence

ORD record
ord-a1aa4a4190e04d639dc516263dcccab9
Source dataset
uspto-grants-1981_01
Patent number
US04243609

Reaction notes

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