tert-Butyl mercaptan → HCID 525387, compound
Reaction equation
[CH2:1](Br)[CH2:2][CH:3]([CH3:5])[CH3:4].[C:7]([SH:11])([CH3:10])([CH3:9])[CH3:8]>>[C:7]([S:11][CH2:1][CH2:2][CH:3]([CH3:5])[CH3:4])([CH3:10])([CH3:9])[CH3:8]Participants
3
Procedure
The title compound was prepared from isoamyl bromide and tert-butyl mercaptan according to the method of Example 1, 86% yield, bp 55°-56° C./7 mm Hg, n20D=1.4460; 1H NMR (CDCl3) δ 0.92 (d, J=6 Hz, 6H, CH3), 1.32 (s, 9H, CH3), 1.45 (q, 2H, CH2), 1.68 (septet, 1H, CH), 2.52 (t, J =6 Hz, 2H, CH2).
Sources & evidence
- ORD record
- ord-4699e2e8629f4d3eacfbfc5cb8c6ec96
- Source dataset
- uspto-grants-1996_10
- Patent number
- US05567849
Reaction notes
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