Diethyl aluminum cyanide → HCID 21541507, compound
Reaction equation
[C:1]([CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][C:12]1[C:13](=[O:23])[CH2:14][CH:15]([O:19][C:20](=[O:22])[CH3:21])[C:16]=1OC)([O:3][CH2:4][CH3:5])=[O:2].[C-:24]#[N:25].C([Al+]CC)C>>[C:1]([CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][C:12]1[C:13](=[O:23])[CH2:14][CH:15]([O:19][C:20](=[O:22])[CH3:21])[C:16]=1[C:24]#[N:25])([O:3][CH2:4][CH3:5])=[O:2]Participants
3
Procedure
According to the procedure similar to that of Step 3 (a) of Example 1, 0.52 g of 2-(6'-carbethoxyhexyl)-3-methoxy-4-acetoxy-2-cyclopenten-1-one prepared in Step 2 was caused to react with diethylaluminum cyanide. Further, the product was purified using chromatography on silica gel to provide 0.25 g of 2-(6'-carbethoxyhexyl)-3-cyano-4-acetoxy-2-cyclopenten-1-one as an oily material.
Workup
- customFurther, the product was purified
Sources & evidence
- ORD record
- ord-767804be100e4eb185b3ba75107a47d1
- Source dataset
- uspto-grants-1976_05
- Patent number
- US03954811
Reaction notes
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