Water → HCID 22016388, compound

HRID 963130Notes

Reaction equation

HRID 963130 reaction equation
[CH2:1]=[CH:2][CH2:3][CH2:4][CH2:5][CH2:6][CH:7]([Si:9]([CH3:12])([CH3:11])Cl)[CH3:8].C(N(CC)CC)C.[OH2:20]>CCOCC>[CH2:1]=[CH:2][CH2:3][CH2:4][CH2:5][CH2:6][CH:7]([Si:9]([CH3:12])([CH3:11])[OH:20])[CH3:8]

Participants

5

Procedure

A solution of 7-oct-1-enyl dimethylchlorosilane (2.56 mL) in ether (2 mL) was added dropwise over 1 hour to a stirring mixture of triethylamine (1.5 mL), water (0.18 mL) and ether (15 mL) in an ice/water bath. The resultant was stirred a further 1 hour in the ice/water bath and filtered washing the filtered solid with ether (10 mL). The filtrate was evaporated with a rotary evaporator and the residue partitioned between hexane (30 mL) and water (30 mL). The organic layer was separated, dried (MgSO4) and filtered through silica gel (70-230 mesh, 60 Å), washing with hexane (100 mL). The filtrate was evaporated with a rotary evaporator to afford a colorless oil which was vacuum dried and weighed (1.06 g).

Workup

  1. filtrationfiltered
  2. washwashing the filtered solid with ether (10 mL)
  3. customThe filtrate was evaporated with a rotary evaporator
  4. customthe residue partitioned between hexane (30 mL) and water (30 mL)
  5. customThe organic layer was separated
  6. dry with materialdried (MgSO4)
  7. filtrationfiltered through silica gel (70-230 mesh, 60 Å)
  8. washwashing with hexane (100 mL)
  9. customThe filtrate was evaporated with a rotary evaporator
  10. customto afford a colorless oil which
  11. customdried

Sources & evidence

ORD record
ord-1f2074081256463cbc94e934ffee5cdc
Source dataset
uspto-grants-1998_06
Patent number
US05763189

Reaction notes

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