Methyl iodide → HCID 19809538, compound

HRID 1632326Notes

Reaction equation

HRID 1632326 reaction equation
[OH:1][CH:2]1[CH2:6][C:5](=[O:7])[C:4]([CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH:13]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[C:14]([OH:16])=[S:15])=[CH:3]1.[C:23](=O)([O-])[O-].[K+].[K+].IC>CC(C)=O>[OH:1][CH:2]1[CH2:6][C:5](=[O:7])[C:4]([CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH:13]([C:17]2[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=2)[C:14]([O:16][CH3:23])=[S:15])=[CH:3]1

Participants

5

Reactant 3

HCID 6328Methyl iodideHCID 11430Potassium CarbonateHCID 178516562HCID 178516562, compound

Product 1

HCID 19809538HCID 19809538, compound

Reagents, catalysts & solvents 1

HCID 180AcetoneSolvent

Procedure

A stirred mixture of 4.38 g. of 7-(4-hydroxycyclopent-2-en-1-on-2-yl)-2-phenylthioheptanoic acid, 1.99 g. of potassium carbonate, 1.63 ml. of iodomethane and 26 ml. of acetone is refluxed for 3.5 hours. The acetone is evaporated and the residue is partitioned between water and ether. The ether layer is washed with brine, dried and concentrated, giving the product as an oily liquid, identified by PMRδ 3.67 (3, s).

Workup

  1. additionA stirred mixture of 4.38 g
  2. customThe acetone is evaporated
  3. customthe residue is partitioned between water and ether
  4. washThe ether layer is washed with brine
  5. customdried
  6. concentrationconcentrated

Sources & evidence

ORD record
ord-08046c61a89d46e5a4a2b90245725746
Source dataset
uspto-grants-1984_10
Patent number
US04474979

Reaction notes

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