Chloroform → 4-Hexadecyloxyphenoxyacetic acid methyl ester

HRID 2227068Notes

Reaction equation

HRID 2227068 reaction equation
[CH2:1]([O:17][C:18]1[CH:23]=[CH:22][C:21]([OH:24])=[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].Br[CH2:26][C:27]([O:29][CH3:30])=[O:28].C(=O)([O-])[O-].[K+].[K+].C(Cl)(Cl)Cl>CC(C)=O>[CH3:30][O:29][C:27](=[O:28])[CH2:26][O:24][C:21]1[CH:22]=[CH:23][C:18]([O:17][CH2:1][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])=[CH:19][CH:20]=1

Participants

6

Procedure

A mixture of 23 g of p-(hexadecyloxy)phenol, 13.35 g of methyl bromoacetate, 10.45 g of potassium carbonate in 200 ml of acetone is refluxed for 24 hours. The mixture is cooled, chloroform added and filtered. The filtrate is evaporated and the residue crystallized from hexane to give 25 g of the desired compound as a gray white solid.

Workup

  1. temperatureis refluxed for 24 hours
  2. temperatureThe mixture is cooled
  3. filtrationfiltered
  4. customThe filtrate is evaporated
  5. customthe residue crystallized from hexane

Sources & evidence

ORD record
ord-94fa9798965742458b4935f25025f0e8
Source dataset
uspto-grants-1994_09
Patent number
US05350759

Reaction notes

Loading…