tert-Butyl methyl ether → (4-Bromo-3-fluorophenyl)(cyclopropyl)sulfane
Reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([SH:8])=[CH:4][C:3]=1[F:9].[CH3:10][C:11]([CH3:14])([O-])C.[K+].BrC1CC1.COC(C)(C)C>CS(C)=O>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([S:8][CH:14]2[CH2:11][CH2:10]2)=[CH:4][C:3]=1[F:9]Participants
6
Conditions
- Temperature
- 90 °C
Procedure
A stirred mixture of 4-bromo-3-fluorobenzenethiol (Preparation 26, 400 mg, 1.93 mmol), potassium tert-butoxide (238 mg, 2.12 mmol) and bromocyclopropane (701 mg, 5.80 mmol) in DMSO (10 mL) was heated at 90° C. for 16 hours. Additional potassium tert-butoxide (43 mg, 0.386 mmol) and bromocyclopropane (467 mg, 3.86 mmol) were added and heating continued at 90° C. for 30 hours. The mixture was cooled to room temperature and poured into 2-methoxy-2-methylpropane (30 mL). The mixture was washed with water (2×30 mL), dried over Na2SO4, concentrated in vacuo and purified by silica gel column chromatography eluting with heptanes to give the title compound as a colourless oil 27% yield, 130 mg.
Workup
- temperatureheating
- temperatureThe mixture was cooled to room temperature
- washThe mixture was washed with water (2×30 mL)
- dry with materialdried over Na2SO4
- concentrationconcentrated in vacuo
- custompurified by silica gel column chromatography
- washeluting with heptanes
Sources & evidence
- ORD record
- ord-818f54f89ddf45ccb0f97de2bd06525e
- Source dataset
- uspto-grants-2015_02
- Patent number
- US08952008B2
Reaction notes
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