Toluene → HCID 19607260, compound
Reaction equation
[CH3:1][CH:2]1[CH2:7][CH2:6][CH2:5][CH:4]([CH3:8])[NH:3]1.C1(C)C=CC=CC=1.[S:16]1[CH2:18][CH2:17]1>>[CH3:1][CH:2]1[CH2:7][CH2:6][CH2:5][CH:4]([CH3:8])[N:3]1[CH2:18][CH2:17][SH:16]Participants
4
Procedure
In a 500 ml three-necked flask 113.2 g(1 mol) of 2,6-dimethylpiperidine in 250 mol toluene was heated at 90° C. Then 60.12 g (1 mol) thiirane is added to the resulting reaction mixture dropwise and the reaction mixture is heated for 5 hours under reflux. The reaction mixture is concentrated in vacuum with a rotary evaporator and is fractionally distilled using a Vigreux column. The yield amounts to 60.55 g of the named compound(35%).
Workup
- temperaturethe reaction mixture is heated for 5 hours
- temperatureunder reflux
- concentrationThe reaction mixture is concentrated in vacuum with a rotary evaporator
- distillationis fractionally distilled
Sources & evidence
- ORD record
- ord-663d6c878c7943aeb80fdaaaf2b0b314
- Source dataset
- uspto-grants-1999_11
- Patent number
- US05985253
Reaction notes
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