3-Chloro-2-butanone → 2,5,6-Trimethyl-2,3-dihydro-1,4-dithiine
Reaction equation
[CH2:1]([SH:5])[CH:2]([SH:4])[CH3:3].Cl[CH:7]([CH3:11])[C:8](=O)[CH3:9]>>[CH3:3][CH:2]1[CH2:1][S:5][C:8]([CH3:9])=[C:7]([CH3:11])[S:4]1Participants
3
Procedure
The procedure of Example 1(a) is repeated, using 1,2-propanedithiol and 3-chloro-2-butanone to give 2,3-dihydro-2,5,6-trimethyl-1,4-dithiin as a clear green liquid, bp 49.5°-51°/0.7 mm, yield 36.5% NMR 1.36 (3d), 1.88 (6s), 2.4-3.6 (3m) (CDCl3). IR, 2905 (sh); 1605, 1410 (broad); 1250, 1155 (sh); 1065 (br); 730, 705.
Sources & evidence
- ORD record
- ord-2d4f7479fab149d8a85cc024eb4535d9
- Source dataset
- uspto-grants-1976_12
- Patent number
- US03997323
Reaction notes
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