Thionyl Chloride → HCID 20505264, compound
Reaction equation
[C:1]1([CH2:7][N:8]2[CH2:12][CH2:11][CH2:10][CH:9]2[CH2:13][CH2:14][OH:15])[CH2:6][CH2:5][CH2:4][CH2:3][CH:2]=1.S(Cl)([Cl:18])=O>C(Cl)(Cl)Cl>[C:1]1([CH2:7][N:8]2[CH2:12][CH2:11][CH2:10][CH:9]2[CH2:13][CH:14]([Cl:18])[OH:15])[CH2:6][CH2:5][CH2:4][CH2:3][CH:2]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
17.8 g of 2-[1-(1-cyclohexenylmethyl) 2-pyrrolidinyl]ethanol (0.085 mole) and 50 ml of chloroform are introduced into a 250 ml balloon flask provided with a stirrer, a thermometer, a condenser and a dropping funnel, then 15.3 ml of thionyl chloride is dropped in, the temperature being kept at about 25°-25° C. by cooling.
Workup
- customprovided with a stirrer
- custombeing kept at about 25°-25° C.
- temperatureby cooling
Sources & evidence
- ORD record
- ord-34ec5c41088649af941509588eead429
- Source dataset
- uspto-grants-1983_04
- Patent number
- US04379161
Reaction notes
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