反応式
[CH3:1][Si:2]([CH3:15])([CH3:14])[C:3]1[CH:13]=[CH:12][C:6]([O:7][Si](C)(C)C)=[CH:5][CH:4]=1.O>C(O)C.Cl>[CH3:1][Si:2]([CH3:15])([CH3:14])[C:3]1[CH:13]=[CH:12][C:6]([OH:7])=[CH:5][CH:4]=1参加物
5
実験手順
28.7 g p-trimethylsilylphenoxytrimethylsilane was dissolved in 9 ml 95 percent ethyl alcohol. One drop of concentrated hydrochloric acid and 4 ml water were added, and the mixture was shaked for 5 minutes. After standing for another 15 minutes, the mixture was washed two times with 30 ml water and separated. The organic phase was poured into a crystallizing dish; p-trimethylsilylphenol crystallized out as white needles. After drying overnight in vacuo, 18.7 g of product was obtained (mp 76 degrees Celsius).
後処理
- waitAfter standing for another 15 minutes
- washthe mixture was washed two times with 30 ml water
- customseparated
- additionThe organic phase was poured into a crystallizing dish
- customp-trimethylsilylphenol crystallized out as white needles
- customAfter drying overnight in vacuo
出典と根拠
- ORDレコード
- ord-45792f8230c445798738aae519ee22a8
- 出典データセット
- uspto-grants-1983_08
- 特許番号
- US04396704
関連ノート
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