1-Octene → Octyltriethoxysilane

HRID 1603258Notes

Reaction equation

HRID 1603258 reaction equation
[CH3:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH:7]=[CH2:8].[CH2:9]([O:11][SiH:12]([O:16][CH2:17][CH3:18])[O:13][CH2:14][CH3:15])[CH3:10].C[Si](OC(=O)C)(OC(=O)C)OC(=O)C>C1(C)C=CC=CC=1>[CH2:8]([Si:12]([O:16][CH2:17][CH3:18])([O:13][CH2:14][CH3:15])[O:11][CH2:9][CH3:10])[CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2][CH3:1]

Participants

5

Reactant 3

HCID 81251-Octene2×HCID 13830TriethoxysilaneHCID 77929Methyltriacetoxysilane

Product 1

HCID 76262OctyltriethoxysilaneYield 91%

Reagents, catalysts & solvents 1

HCID 1140TolueneSolvent2×

Conditions

Temperature
50 °C

Procedure

224 mg Of octene-1, 328 mg of triethoxysilane, and 56 mg of toluene were placed in a glass reaction tube and 4 mg of methyltriacetoxysilane were added. Then, 0.001 ml of a toluene solution of a 0-valent platinum complex of divinyltetramethylsiloxane (platinum content: 0.4 wt %) was added to this mixture. The reaction tube was sealed with Teflon tape and heated for 30 minutes in an oil bath at 50° C. When the contents were analyzed by GC-MS following cooling, the conversion rate of octene-1 was 97.6% and n-octyltriethoxysilane was produced at a yield of 91%.

Workup

  1. additionwere added
  2. temperaturefollowing cooling

Sources & evidence

ORD record
ord-3346628737064ae4b5d150c3a92f1ef3
Source dataset
uspto-grants-1999_11
Patent number
US05986124

Reaction notes

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