Water → HCID 53925496, compound

HRID 1704346Notes

Reaction equation

HRID 1704346 reaction equation
[C:1]1([CH3:11])[CH:6]=[CH:5][C:4]([S:7](Cl)(=[O:9])=[O:8])=[CH:3][CH:2]=1.[C:12]([O:15][CH:16]([CH2:21][O:22][C:23]1[CH:28]=[CH:27][C:26]([F:29])=[CH:25][CH:24]=1)[CH2:17][CH2:18][CH2:19][OH:20])(=[O:14])[CH3:13].O>N1C=CC=CC=1.CCOCC>[S:7]([O:20][CH2:19][CH2:18][CH2:17][CH:16]([O:15][C:12](=[O:14])[CH3:13])[CH2:21][O:22][C:23]1[CH:28]=[CH:27][C:26]([F:29])=[CH:25][CH:24]=1)([C:4]1[CH:5]=[CH:6][C:1]([CH3:11])=[CH:2][CH:3]=1)(=[O:9])=[O:8]

Participants

6

Reactant 3

HCID 962Water2×HCID 73974-Toluenesulfonyl chlorideHCID 22759227HCID 22759227, compound

Product 1

HCID 53925496HCID 53925496, compoundYield 93%

Reagents, catalysts & solvents 2

HCID 1049PyridineSolventHCID 3283Diethyl EtherSolvent

Procedure

A solution of p-toluenesulfonyl chloride (42.0 g., 0.22 mole) in pyridine (100 ml.) is cooled in an ice bath while 4-acetoxy-5-(4-fluorophenoxy)-1-pentanol (49.7 g., 0.193 mole) is added dropwise with stirring during 40 minutes. The ice bath is replaced by a cool (20°) water and stirring is continued for 2 hours. The mixture is then poured into 500 ml. of water. The oily product is taken up in ether, washed with 2N hydrochloric acid and water and dried over sodium sulfate. The solvent is distilled in vacuo to leave 73.5 g. (93%) of the crude title compound as a yellow oil.

Workup

  1. additionis added dropwise
  2. stirringstirring
  3. waitis continued for 2 hours
  4. additionThe mixture is then poured into 500 ml
  5. washwashed with 2N hydrochloric acid and water
  6. dry with materialdried over sodium sulfate
  7. distillationThe solvent is distilled in vacuo
  8. customto leave 73.5 g

Sources & evidence

ORD record
ord-d4baaf2382b143fe93b38710fa764e1c
Source dataset
uspto-grants-1978_11
Patent number
US04126629

Reaction notes

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