Tributylstannane → 1-(tributylstannyl)-1E-undecen-3-ol
Reaction equation
[CH:1]#[C:2][CH:3]([OH:12])[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH3:11].[CH2:13]([SnH:17]([CH2:22][CH2:23][CH2:24][CH3:25])[CH2:18][CH2:19][CH2:20][CH3:21])[CH2:14][CH2:15][CH3:16]>>[CH2:22]([Sn:17]([CH2:13][CH2:14][CH2:15][CH3:16])([CH2:18][CH2:19][CH2:20][CH3:21])/[CH:1]=[CH:2]/[CH:3]([OH:12])[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH3:11])[CH2:23][CH2:24][CH3:25]Participants
3
Conditions
- Temperature
- 120 °C
Procedure
To 0.07 g (0.42 mmol) of the titled product of Example 7 is added 0.15 g (0.5 mmol) of tri-n-butyltin hydride and 20 mg of azoisobutyronitrile (AIBN). The reaction mixture was heated to 120° C. for 2 hours. Afterwards, it was cooled to room temperature and pumped at high vacuum overnight. The crude reaction mixture was then heated to 90° C. and maintained at high vacuum for 2 additional hours. Upon cooling to room temperature, the crude product was used as is.
Workup
- temperatureAfterwards, it was cooled to room temperature
- custompumped at high vacuum overnight
- customThe crude reaction mixture
- temperaturewas then heated to 90° C.
- temperaturemaintained at high vacuum for 2 additional hours
- temperatureUpon cooling to room temperature
Sources & evidence
- ORD record
- ord-1c275844a8354614ab54f2b7bfa78c94
- Source dataset
- uspto-grants-1990_11
- Patent number
- US04970234
Reaction notes
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