Acetic Acid → HCID 19087517, compound

HRID 1464243Notes

Reaction equation

HRID 1464243 reaction equation
[S:1]1[C:5](=[O:6])[CH2:4][C:3]2[CH:7]=[CH:8][CH:9]=[CH:10][C:2]1=2.[OH-].[Na+].[Cl:13][C:14]1[CH:21]=[CH:20][C:17]([CH2:18]Cl)=[CH:16][CH:15]=1.C(O)(=[O:24])C>O>[Cl:13][C:14]1[CH:21]=[CH:20][C:17]([CH2:18][S:1][C:2]2[CH:10]=[CH:9][CH:8]=[CH:7][C:3]=2[CH2:4][C:5]([OH:24])=[O:6])=[CH:16][CH:15]=1

Participants

6

Reactant 4

HCID 176Acetic AcidHCID 77231-Chloro-4-(chloromethyl)benzeneHCID 14798Sodium HydroxideHCID 591560Benzo[b]thiophen-2(3H)-one

Product 1

HCID 19087517HCID 19087517, compound

Reagents, catalysts & solvents 1

HCID 962WaterSolvent2×

Procedure

Benzo[b]thiophen-2(3H)-one (6g) and sodium hydroxide (3.2 g) were refluxed in water (40 ml) for one hour. 4-Chlorobenzyl chloride (6.44 g was added and the mixture refluxed for a further 11/2 hours and allowed to cool overnight. Water (25 ml) was added, followed by acetic acid (100 ml). The solid was collected, washed with water and dried to give [2-(4-chlorobenzylthio)phenyl]acetic acid, m.p. 149°-51°. A solution of this product 10.4 g) in methanol (250 ml) containing concentrated sulphuric acid (0.5 ml) was heated under reflux overnight and excess methanol evaporated. Ether and water were added and the organic phase was washed with aqueous sodium hydroxide, dried and evaporated. The product which solidified was re-crystallised from hexane to give the methyl ester of the starting acid, m.p. 52°-4°. This was treated with methyl formate and sodium hydride in a similar manner to the procedure described in Example 1 to give methyl (E)-3-methoxy-2 -[2-(4-chlorobenzylthio)phenyl]prop-2-enoate, m.p. 81°-4°, (Compound 3) and the corresponding Z-isomer, m.p. 127°-8°. (Compound 4), which were separated by silica gel column chromatography.

Workup

  1. temperaturethe mixture refluxed for a further 11/2 hours
  2. temperatureto cool overnight
  3. customThe solid was collected
  4. washwashed with water
  5. customdried

Sources & evidence

ORD record
ord-4521e6d566db4b76b9330ed8832cf277
Source dataset
uspto-grants-1994_04
Patent number
US05304530

Reaction notes

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