4-Toluenesulfonyl chloride → HCID 53673877, compound

HRID 127806Notes

Reaction equation

HRID 127806 reaction equation
[CH:1]([O:5][C:6](=[O:16])[CH2:7][CH:8]([CH3:15])[CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][OH:14])([CH2:3][CH3:4])[CH3:2].[C:17]1([CH3:27])[CH:22]=[CH:21][C:20]([S:23](Cl)(=[O:25])=[O:24])=[CH:19][CH:18]=1>N1C=CC=CC=1>[CH:1]([O:5][C:6](=[O:16])[CH2:7][CH:8]([CH3:15])[CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][O:14][S:23]([C:20]1[CH:21]=[CH:22][C:17]([CH3:27])=[CH:18][CH:19]=1)(=[O:25])=[O:24])([CH2:3][CH3:4])[CH3:2]

Participants

4

Procedure

A mixture of the oily ester, thus obtained, one ml of pyridine and 485 mg of p-toluenesulphonyl chloride was stirred at room temperature for 16 hours. The reaction mixture was poured into ice-water, extracted with ethyl acetate, the extract washed with dilute sulphuric acid, a saturated aqueous solution of sodium bicarbonate, a saturated aqueous solution of sodium chloride, dried over magnesium sulphate and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel using a mixture of methylene chloride and ethyl acetate (20:1) as eluent to give 647 mg of the subtitle compound having the following physical characteristics:

Workup

  1. customthus obtained
  2. extractionextracted with ethyl acetate
  3. washthe extract washed with dilute sulphuric acid
  4. dry with materiala saturated aqueous solution of sodium bicarbonate, a saturated aqueous solution of sodium chloride, dried over magnesium sulphate
  5. concentrationconcentrated under reduced pressure
  6. customThe residue was purified by column chromatography on silica gel using
  7. additiona mixture of methylene chloride and ethyl acetate (20:1) as eluent

Sources & evidence

ORD record
ord-ecfc39179b38456085ef898392faca12
Source dataset
uspto-grants-1981_03
Patent number
US04256757

Reaction notes

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