Benzoate → HCID 18609748, compound

HRID 2309132Notes

Reaction equation

HRID 2309132 reaction equation
[C:1](Cl)(=O)[C:2]1[CH:7]=[CH:6]C=[CH:4][CH:3]=1.S(=O)(=O)(O)O.[C:15](=[O:18])(O)[O-].[Na+].[C:20]([O-:28])(=[O:27])[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1.[CH3:29][CH2:30][O:31][CH2:32][CH3:33]>O.N1C=CC=CC=1>[C:20]([O:28][C@@H:4]1[CH2:3][C@H:2]2[C@H:7]([CH2:6][C:15](=[O:18])[CH2:1]2)[C@H:29]1[CH2:30][O:31][CH2:32][C:33]1[CH:6]=[CH:7][CH:2]=[CH:3][CH:4]=1)(=[O:27])[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1

Participants

8

Procedure

A solution of 0.55 g. of the alcohol prepared according to Reference Example 1(m) in 4 ml. of pyridine is combined with 0.5 ml. of benzoyl chloride. The mixture is agitated for 4 hours at 25°, combined with 0.4 ml. of water, agitated for 2 hours, diluted with ether, and the mixture is shaken in succession with water, 5% sulfuric acid, water, 4% sodium bicarbonate solution, and three times with water. After drying over magnesium sulfate the mixture is evaporated under vacuum, thus obtaining 720 mg. of the benzoate as a colorless oil.

Workup

  1. dry with materialAfter drying over magnesium sulfate the mixture
  2. customis evaporated under vacuum
  3. customthus obtaining 720 mg

Sources & evidence

ORD record
ord-2e7ea231346b41a39c3c2801b867ee0d
Source dataset
uspto-grants-1987_09
Patent number
US04692464

Reaction notes

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