Methanethiol → HCID 13505578, compound
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
Reactant 4
Product 1
Reagents, catalysts & solvents 1
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 2.5N 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
- temperaturewith cooling in an ice bath
- temperatureThe solution was heated
- customMost of the methanol was evaporated under reduced pressure
- extractionThe precipitated oil was extracted with ether (3×)
- washThe ether extracts were washed with water, saturated brine
- dry with materialdried over MgSO4
- customRemoval of the ether under reduced pressure
- customgave a colorless oil that
- customcrystallized
- customIt was recrystallized from ether-hexane
Sources & evidence
- ORD record
- ord-41280cefcf51421d82d08af8b9125879
- Source dataset
- uspto-grants-1991_12
- Patent number
- US05071843
Reaction notes
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