Ethyl Thioglycolate → 5-(Carbethoxymethylthio)-1-(2-furyl)-1-pentanol

HRID 1395318Notes

Reaction equation

HRID 1395318 reaction equation
[SH:1][CH2:2][C:3]([O:5][CH2:6][CH3:7])=[O:4].Cl[CH2:9][CH2:10][CH2:11][CH2:12][CH:13]([C:15]1[O:16][CH:17]=[CH:18][CH:19]=1)[OH:14].[O-]CC.[Na+]>C(O)C>[C:3]([CH2:2][S:1][CH2:9][CH2:10][CH2:11][CH2:12][CH:13]([C:15]1[O:16][CH:17]=[CH:18][CH:19]=1)[OH:14])([O:5][CH2:6][CH3:7])=[O:4]

Participants

5

Reactant 3

HCID 12185Ethyl ThioglycolateHCID 2723922Sodium ethoxide2×HCID 202925795-Chloro-1-(2-furyl)-1-pentanol

Product 1

HCID 202925745-(Carbethoxymethylthio)-1-(2-furyl)-1-pentanol

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

To a stirred, refluxing mixture of 76 g of ethyl mercaptoacetate, 79.5 g of 5-chloro-1-(2-furyl)-1-pentanol and 10 ml of 1.5M sodium ethoxide in ethanol is added an additional 300 ml of 1.5m sodium ethoxide during 15 minutes. The resulting mixture is stirred at reflux for 3 hours, cooled, and concentrated to remove most of the ethanol. The residue is partitioned with ether and water. The ether phase is washed with brine and dried over potassium carbonate. The solution is concentrated, diluted with xylene, and again concentrated to give an oil, pmr spectrum (CDCl3): δ 3.24 (singlet, --S--CH2CO2C2H5) and 4.70 (triplet, CH2CHOH).

Workup

  1. temperatureTo a stirred, refluxing
  2. temperatureat reflux for 3 hours
  3. temperaturecooled
  4. concentrationconcentrated
  5. customto remove most of the ethanol
  6. customThe residue is partitioned with ether and water
  7. washThe ether phase is washed with brine
  8. dry with materialdried over potassium carbonate
  9. concentrationThe solution is concentrated
  10. additiondiluted with xylene
  11. concentrationagain concentrated
  12. customto give an oil, pmr spectrum (CDCl3)

Sources & evidence

ORD record
ord-35a09a5677cc4b07bb686ec8e505e3f7
Source dataset
uspto-grants-1980_05
Patent number
US04202988

Reaction notes

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