Butanethiol → HCID 11045673, compound
Reaction equation
[C:1]1([CH:7]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[C:8]([N:10]=[C:11]=[O:12])=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH2:19]([SH:23])[CH2:20][CH2:21][CH3:22]>>[CH2:19]([S:23][C:11](=[O:12])[NH:10][C:8](=[O:9])[CH:7]([C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)[C:1]1[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1)[CH2:20][CH2:21][CH3:22]Participants
3
Procedure
The title compound, white solid, m.p.=99° C. and MS: m/e=327 (M+) was prepared in accordance with the general method of example 1 from diphenylacetyl isocyanate and butanethiol.
Sources & evidence
- ORD record
- ord-1c1d0c2976af4325b6811f87bf67430f
- Source dataset
- uspto-grants-2004_10
- Patent number
- US06803381B1
Reaction notes
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