Methanethiol → HCID 13505578, compound

HRID 1638522Notes

Reaction equation

HRID 1638522 reaction equation
[CH3:1][SH:2].C[O-].[Na+].Br[CH2:7][CH2:8][CH2:9][CH2:10][CH2:11]/[CH:12]=[C:13](\[NH:17][C:18]([CH:20]1[CH2:22][C:21]1([CH3:24])[CH3:23])=[O:19])/[C:14]([OH:16])=[O:15].N#N>CO>[CH3:23][C:21]1([CH3:24])[CH2:22][CH:20]1[C:18]([NH:17]/[C:13](=[CH:12]\[CH2:11][CH2:10][CH2:9][CH2:8][CH2:7][S:2][CH3:1])/[C:14]([OH:16])=[O:15])=[O:19]

Participants

6

Procedure

A stream of CH3SH gas was bubbled through a solution of 162 mg (3 mmoles) of sodium methoxide in 5 ml of methanol for 10 min. with cooling in an ice bath. The solution was allowed to warm to room temperature and 332 mg (1 mmole) of Z-8-bromo-2-(2,2-dimethylcyclopropanecarboxamido)-2-octenoic acid was added. The solution was heated under reflux for 30 min. in a N2 atmosphere. Most of the methanol was evaporated under reduced pressure, the residue 2.5 N HCl. The precipitated oil was extracted with ether (3×). The ether extracts were washed with water, saturated brine and dried over MgSO4. Removal of the ether under reduced pressure gave a colorless oil that crystallized upon standing. It was recrystallized from ether-hexane to give 178 mg of Z-2-(2,2-dimethylcyclopropanecarboxamido)-8-methylthio-2-octenoic acid, m.p. 82°-84° C. Homogeneous by TLC (toluene-acetic acid, 4:1). The NMR spectrum was in accord with the desired structure.

Workup

  1. temperaturewith cooling in an ice bath
  2. temperatureThe solution was heated
  3. customMost of the methanol was evaporated under reduced pressure
  4. extractionThe precipitated oil was extracted with ether (3×)
  5. washThe ether extracts were washed with water, saturated brine
  6. dry with materialdried over MgSO4
  7. customRemoval of the ether under reduced pressure
  8. customgave a colorless oil that
  9. customcrystallized
  10. customIt was recrystallized from ether-hexane

Sources & evidence

ORD record
ord-6f2921e6fa9a41778b9194069d684017
Source dataset
uspto-grants-1989_11
Patent number
US04880793

Reaction notes

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