Reaction equation
Cl[CH:2]1[CH2:7][CH2:6][CH2:5][CH2:4][C:3]1=O.[CH2:9]([SH:13])[CH:10]([SH:12])[CH3:11]>>[CH3:11][CH:10]1[S:12][C:3]2[CH2:4][CH2:5][CH2:6][CH2:7][C:2]=2[S:13][CH2:9]1Participants
3
Procedure
The procedure of Example 1(a) is followed using 2-chloro-cyclohexanone and 1,2-propanedithiol to give 5,6,7,8-tetrahydro-2-methyl-1,4-benzodithian as a greenish oil, bp 127°-130°/2.3 mm, Yield 66%. NMR, 1.36 (3d), 1.4-1.88 (4m), 1.88-2.3 (4m), 2.6-3.7 (3m). IR, 2920, 1615, 1410, 1325, 1250, 1120, 855, 715.
Sources & evidence
- ORD record
- ord-2640805192e147a7b02aead68d072e33
- Source dataset
- uspto-grants-1976_12
- Patent number
- US03997323
Linked notes
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