Tert-Butyl hypochlorite → HCID 20222972, compound
Reaction equation
[NH2:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][C:11]=1[CH3:12])[C:8](=[O:13])[CH2:7][CH2:6][CH2:5]2.[Cl:14]OC(C)(C)C>O1CCCC1>[NH2:1][C:2]1[C:3]([Cl:14])=[C:4]2[C:9](=[CH:10][C:11]=1[CH3:12])[C:8](=[O:13])[CH2:7][CH2:6][CH2:5]2Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The product from Example 105 (0.175 g) was dissolved in tetrahydrofuran (5 ml) and was treated with t-butyl hypochlorite (0.12 ml). Following the procedure of Example 95 the desired product was obtained in 90% yield.
Sources & evidence
- ORD record
- ord-810634ec6dfa472abb3a38492e38a468
- Source dataset
- uspto-grants-1987_01
- Patent number
- US04634705
Reaction notes
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