Iodine → 1-Iodo-4-trimethylsiloxy-trans-1-octene
Reaction equation
CC(C)C(BC(C(C)C)C)C.[CH3:12][Si:13]([CH3:24])([CH3:23])[O:14][CH:15]([CH2:19][CH2:20][CH2:21][CH3:22])[CH2:16][C:17]#[CH:18].C[N+]([O-])(C)C.[OH-].[Na+].[I:32]I>O1CCCC1>[I:32]/[CH:18]=[CH:17]/[CH2:16][CH:15]([O:14][Si:13]([CH3:23])([CH3:24])[CH3:12])[CH2:19][CH2:20][CH2:21][CH3:22]Participants
Procedure
To a stirred solution of 0.20 moles of freshely prepared bis-(3-methyl-2-butyl)borane in 300 ml of tetrahydrofuran at 0°-5° C. is added dropwise a solution of 19.8 g of 4-trimethylsiloxy-1-octyne in 30 ml of tetrahydrofuran. The resulting mixture is stirred at ambient temperature for several hours, cooled in an ice bath, and treated with 53 g of trimethylamine oxide. The mixture is stirred several hours at 25°-40° C. and then poured into 2 liters of 15% sodium hydroxide. The resulting mixture is treated immediately with a solution of 140 g of iodine in 300 ml of tetrahydrofuran. After 0.5 hour the organic phase is-separated and the aqueous phase is extracted with ether. The combined organic layers are washed with water, sodium thiosulfate solution, and brine; dried over magnesium sulfate; and concentrated to give an oil, pmr spectrum (CDCl3): 6.2 (d, ICH=) and 6.7 (quintuplet, =CH--).
Workup
- temperaturecooled in an ice bath
- stirringThe mixture is stirred several hours at 25°-40° C.
- customAfter 0.5 hour the organic phase is-separated
- extractionthe aqueous phase is extracted with ether
- washThe combined organic layers are washed with water, sodium thiosulfate solution, and brine
- dry with materialdried over magnesium sulfate
- concentrationand concentrated
- customto give an oil, pmr spectrum (CDCl3)
Sources & evidence
- ORD record
- ord-7f822d332743491a9414814b702c45de
- Source dataset
- uspto-grants-1979_08
- Patent number
- US04165331
Reaction notes
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