Ethanol → HCID 178448250, compound
Reaction equation
[CH2:1]([Sn:5](=[O:10])[CH2:6][CH2:7][CH2:8][CH3:9])[CH2:2][CH2:3][CH3:4].[CH2:11]([Sn:15](N=C=S)([N:20]=[C:21]=[S:22])[CH2:16][CH2:17][CH2:18][CH3:19])[CH2:12][CH2:13][CH3:14].C([OH:28])C>>[OH:10][Sn:5]([CH2:6][CH2:7][CH2:8][CH3:9])([CH2:1][CH2:2][CH2:3][CH3:4])[O:28][Sn:15]([CH2:16][CH2:17][CH2:18][CH3:19])([CH2:11][CH2:12][CH2:13][CH3:14])[N:20]=[C:21]=[S:22]Participants
4
Procedure
A mixture of di-n-butyltin oxide (2.14 g, 8.6 mmol) and di-n-butyltin diisothiocyanate (1.0 g, 2.8 mmol) in ethanol (30 mL) was heated to reflux for 6 hours during which time the white slurry became a clear solution. The reaction mixture was concentrated via rotary evaporator to a solid which was pulverized and left exposed at ambient temperature for 18 hours. The powder was recrystallized from hexanes at 0° C. to give the title compound as a white solid (2.74 g, 86%).
Workup
- temperaturewas heated
- temperatureto reflux for 6 hours during which time the white slurry
- concentrationThe reaction mixture was concentrated via rotary evaporator to a solid which
- waitleft
- customThe powder was recrystallized from hexanes at 0° C.
Sources & evidence
- ORD record
- ord-89ac5b06b9644b588ff3d93b8472253a
- Source dataset
- uspto-grants-2001_11
- Patent number
- US06313290B1
Reaction notes
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