反応式
P(Br)(Br)[Br:2].N1C=CC=CC=1.[OH:11][C:12]1[CH:19]=[CH:18][C:15]([CH2:16]O)=[CH:14][CH:13]=1>C1COCC1>[OH:11][C:12]1[CH:19]=[CH:18][C:15]([CH2:16][Br:2])=[CH:14][CH:13]=1参加物
5
反応条件
- 温度
- -20 °C
実験手順
To a stirred solution of PBr3 (1.38 g, 5.0 mmol) in dry THF (2 ml) at −5° C. was added a solution of dry pyridine (0.201 ml) in dry THF (0.4 ml). A solution of 4-Hydroxybenzyl alcohol (1.89 g, 15.2 mmol) in dry THF (23 ml) was added drop wise to the reaction mixture. The reaction mixture was allowed to stand at room temperature for 18 hours, then diluted with THF and filtered through celite pad. The filtrate was evaporated, the resulting semisolid was redissolved in dry toluene (16 ml). The solution was maintained at −20° C. for 2 hours, and then filtered through celite pad to provide the title compound as a light yellow solution which was used without further purification.
後処理
- filtrationfiltered through celite pad
- customThe filtrate was evaporated
- dissolutionthe resulting semisolid was redissolved in dry toluene (16 ml)
- filtrationfiltered through celite pad
出典と根拠
- ORDレコード
- ord-7b0b35eb3ff04b7a9a9875af0715cb58
- 出典データセット
- uspto-grants-2005_02
- 特許番号
- US06858602B2
関連ノート
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