Methanol → HCID 19782774, compound
Reaction equation
[C:1]([SH:5])([CH3:4])([CH3:3])[CH3:2].[OH-].[Na+].CO.Br[CH:11]([CH2:14][CH2:15]Cl)[CH:12]=[O:13]>O>[CH:12]([C:11]1([S:5][C:1]([CH3:4])([CH3:3])[CH3:2])[CH2:15][CH2:14]1)=[O:13]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
Under an atmosphere of nitrogen and while cooling with ice, 112 ml of tert-butyl mercaptan are added dropwise over 10 minutes to a solution, cooled to 5° C., of 80 g of sodium hydroxide in 750 ml of water. Then 50 ml of methanol are added. After 1 hour, 151 g of 2-bromo-4-chlorobutanal (89.5%) are added dropwise over 15 minutes with efficient stirring and cooling, whereupon the temperature of the reaction mixture rises from 5° to 20° C. After 30 minutes, the mixture is extracted 4 times with diethyl ether. The combined organic phases are washed twice with a saturated solution of sodium chloride and dried over magnesium sulfate. The residue obtained after concentrating the residue on a rotary evaporator is fractionated over a 30 cm packed column, affording 89 g of 1-formyl-1-tert-butylthiocyclopropane in 89% purity. Boiling point: 112°-114° C./8 400 Pa.
Workup
- additionare added dropwise over 10 minutes to a solution
- temperaturecooling, whereupon the temperature of the reaction mixture
- customrises from 5° to 20° C
- waitAfter 30 minutes
- extractionthe mixture is extracted 4 times with diethyl ether
- washThe combined organic phases are washed twice with a saturated solution of sodium chloride
- dry with materialdried over magnesium sulfate
- customThe residue obtained
- concentrationafter concentrating the residue
- customon a rotary evaporator
Sources & evidence
- ORD record
- ord-748eb51832274454bc948270118bc1d8
- Source dataset
- uspto-grants-1993_11
- Patent number
- US05264630
Reaction notes
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