反応式
O[C:2]1[CH:9]=[CH:8][C:5]([CH2:6][OH:7])=[CH:4][CH:3]=1.[OH-:10].[Na+].Br[CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH:21]=[CH2:22]>C(O)C>[CH2:13]([O:7][CH:6]([OH:10])[C:5]1[CH:8]=[CH:9][CH:2]=[CH:3][CH:4]=1)[CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH:21]=[CH2:22]参加物
反応条件
- 温度
- 65 °C
実験手順
First, 12.80 g (0.10 M) of 4-hydroxybenzyl alcohol (compound (8)) was dissolved in ethanol 190 mL, and 4.0 g (0.10 M) of sodium hydroxide was added thereto. The resulting mixture was heated to 65° C. After heating, 24.14 g (0.11 M) of 10-bromo-1-decene (compound (22)) prepared in Synthetic example 1-1 was added dropwise, and the resulting mixture was aged at a mixture temperature of 76° C. for 6 hours. Next, the generated salt was removed by decantation, and the reaction solution was concentrated. After concentration, the resulting solution was diluted with 350 mL of diethyl ether and washed twice with 100 mL of deionized water. After washing, the organic layer was concentrated to produce crude crystals. The crude crystals were recrystallized twice from 25 mL of hexane. The recrystallized crystals were washed with hexane and dried. Thereby, 16.88 g of 9-decenoxybenzyl alcohol (compound (23)) was produced (yield: 64.3%).
後処理
- temperatureAfter heating
- additionwas added dropwise
- customNext, the generated salt was removed by decantation
- concentrationthe reaction solution was concentrated
- concentrationAfter concentration
- additionthe resulting solution was diluted with 350 mL of diethyl ether
- washwashed twice with 100 mL of deionized water
- washAfter washing
- concentrationthe organic layer was concentrated
- customto produce crude crystals
- customThe crude crystals were recrystallized twice from 25 mL of hexane
- washThe recrystallized crystals were washed with hexane
- customdried
出典と根拠
- ORDレコード
- ord-1670db7048ab4080a5971293dfce708a
- 出典データセット
- uspto-grants-2008_06
- 特許番号
- US07390433B2
関連ノート
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