Thioglycolic Acid → HCID 40476034, compound

HRID 1655422Notes

Reaction equation

HRID 1655422 reaction equation
[SH:1][CH2:2][C:3]([OH:5])=[O:4].C[O-].[Na+].[CH:9]12[O:15][CH:10]1[CH2:11][CH2:12][CH2:13][CH2:14]2>CO>[OH:15][C@@H:10]1[CH2:11][CH2:12][CH2:13][CH2:14][C@H:9]1[S:1][CH2:2][C:3]([OH:5])=[O:4]

Participants

5

Procedure

Mercaptoacetic acid (18.5 g), 0.20 mole) was added to methanol (125 ml) containing sodium methoxide [prepared from sodium (9.3 g, 0.40 mole)] cooled by an ice bath. After 20 minutes, cyclohexene oxide was added slowly during 20 minutes. The ice bath was removed, and the reaction mixture was stirred at room temperature for 4 hours at which time it was poured into water (250 ml) containing concentrated hydrochloric acid (50 ml) and brine (200 ml). The reaction mixture was extracted three times with 150 ml of diethyl ether. The combined diethyl ether extracts were washed twice with 50 ml of brine, dried over anhydrous magnesium sulfate, filtered and concentrated with a rotary evaporator to give the product as an oil. The structure was supported by NMR.

Workup

  1. temperaturecooled by an ice bath
  2. customThe ice bath was removed
  3. additionwas poured into water (250 ml)
  4. additioncontaining concentrated hydrochloric acid (50 ml) and brine (200 ml)
  5. extractionThe reaction mixture was extracted three times with 150 ml of diethyl ether
  6. washThe combined diethyl ether extracts were washed twice with 50 ml of brine
  7. dry with materialdried over anhydrous magnesium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated with a rotary evaporator

Sources & evidence

ORD record
ord-cb0cc10a777a4ba0a6ab1c70889dea98
Source dataset
uspto-grants-1993_10
Patent number
US05250567

Reaction notes

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