Hexyl isocyanate → HCID 131729124, compound
Reaction equation
[Br:1][C:2]1[CH:11]=[CH:10][C:5]2[NH:6][C:7](=[O:9])[S:8][C:4]=2[CH:3]=1.N([CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH3:20])=C=O>O1CCOCC1>[Br:1][C:2]1[CH:11]=[CH:10][C:5]2[NH:6][C:7](=[O:9])[S:8][C:4]=2[CH:3]=1.[CH3:20][CH2:19][CH:18]([C:7]([NH2:6])=[O:9])[CH2:17][CH2:16][CH3:15]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
200 mg (0.869 mmol) of 6-bromo-3H-benzothiazol-2-one were reacted in analogy to Example 1 with 132.7 mg (1.04 mmol) of 1-isocyanatohexane in dioxane at 80° C. Yield: 185 mg (59%), M+H+: 357.1.
Sources & evidence
- ORD record
- ord-3a65384ff267459d85bcfde798e233fb
- Source dataset
- uspto-grants-2011_08
- Patent number
- US08008331B2
Reaction notes
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