Formaldehyde → 2',3'-Dichloro-4'-methylthio-2-cyclopentylacrylophenone
Reaction equation
[Cl:1][C:2]1[C:7]([Cl:8])=[C:6]([S:9][CH3:10])[CH:5]=[CH:4][C:3]=1[C:11](=[O:18])[CH2:12][CH:13]1[CH2:17][CH2:16][CH2:15][CH2:14]1.[CH2:19]=O.S(=O)(=O)(O)O>O1CCOCC1>[Cl:1][C:2]1[C:7]([Cl:8])=[C:6]([S:9][CH3:10])[CH:5]=[CH:4][C:3]=1[C:11](=[O:18])[C:12]([CH:13]1[CH2:14][CH2:15][CH2:16][CH2:17]1)=[CH2:19]Participants
5
Procedure
2',3'-dichloro-4'-methylthio-2-cyclopentylacrylophenone is prepared following substantially the same procedure described in Example 3, Step B, using the following substances: 2',3'-dichloro-4'-methylthio-2-cyclopentylacetophenone (54.5 g., 0.18 mole), paraformaldehyde (21.6 g., 0.72 mole), concentrated sulfuric acid (9.65 g.) and dioxane (450 ml.).
Sources & evidence
- ORD record
- ord-8b9de3dec3c8441a867aa0d9fc4dc098
- Source dataset
- uspto-grants-1977_03
- Patent number
- US04012524
Reaction notes
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