Dimethyl Sulfoxide → HCID 86752368, compound
Reaction equation
C(Cl)(=O)C(Cl)=O.CS(C)=O.[OH:11][CH2:12][C@@H:13]1[C@@H:19]([C:20]2[CH:25]=[CH:24][C:23]([Cl:26])=[C:22]([Cl:27])[CH:21]=2)[CH2:18][C@H:17]2[N:28]([CH3:29])[C@@H:14]1[CH2:15][CH2:16]2.C(N(CC)CC)C>C(Cl)Cl>[CH:12]([C@@H:13]1[C@@H:19]([C:20]2[CH:25]=[CH:24][C:23]([Cl:26])=[C:22]([Cl:27])[CH:21]=2)[CH2:18][C@H:17]2[N:28]([CH3:29])[C@@H:14]1[CH2:15][CH2:16]2)=[O:11]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of oxalylchloride (2.3 ml) in absolute methylene chloride (60 ml) at -60° C., a solution of dimethylsulphoxide (4 ml) in absolute methylene chloride (10 ml) was added over 10 minutes. The mixture was stirred for 10 minutes and a suspension of (1R,2R,3S)-2-hydroxymethyl-3-(3,4-dichlorophenyl)tropane (7 g, 23.3 mmol) in absolute methylene chloride (400 ml) was added over 15 minutes. The resulting mixture was stirred for 10 minutes followed by addition of triethylamine (17 ml, 0.12 mmol) and stirring for another 10 minutes. The reaction mixture was allowed to reach ambient temperature and was quenched by addition of water (200 ml). The organic phase was washed twice with water, dried and concentrated in vacuo yielding the title compound as white crystals, m.p. 131°-135° C.
Workup
- additionwas added over 15 minutes
- stirringThe resulting mixture was stirred for 10 minutes
- stirringstirring for another 10 minutes
- customto reach ambient temperature
- customwas quenched by addition of water (200 ml)
- washThe organic phase was washed twice with water
- customdried
- concentrationconcentrated in vacuo
Sources & evidence
- ORD record
- ord-fd79ae60a68548ab9a6af102d7719b32
- Source dataset
- uspto-grants-1998_04
- Patent number
- US05736556
Reaction notes
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