反応式
[F:1][C:2]1[CH:9]=[CH:8][C:7]([OH:10])=[CH:6][C:3]=1[CH:4]=[O:5].FC1C=CC(OC)=CC=1C=O.B(Br)(Br)Br>ClCCl>[F:1][C:2]1[CH:9]=[CH:8][C:7]([OH:10])=[CH:6][C:3]=1[CH2:4][OH:5]参加物
5
実験手順
2-Fluoro-5-hydroxybenzyl alcohol was prepared according to the following procedure: 2-Fluoro-5-hydroxybenzaldehyde: to a stirred solution of 2-fluoro-5-methoxybenzaldehyde (18.3 g) in dichloromethane (200 mL) at 0° C. was added dropwise a solution of boron tribromide in dichloromethane (1M, 120 mL, 1 eq.). The mixture was stirred for 3 h then concentrated to a volume of ˜50 mL and partitioned between ethyl acetate (500 mL) and water (500 mL). The organic layer was washed (water), dried (magnesium sulfate) and concentrated to give a red oil (22.7 g). The oil was purified by column chromatography (SiO2, DCM→DIPE) to give the product as a pink crystalline solid (9.9 g, 59% yield);
後処理
- concentrationthen concentrated to a volume of ˜50 mL
- custompartitioned between ethyl acetate (500 mL) and water (500 mL)
- washThe organic layer was washed (water)
- dry with materialdried (magnesium sulfate)
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-dc884d24ad0149bc9a26ea2ecdad2a09
- 出典データセット
- uspto-grants-2006_04
- 特許番号
- US07022707B2
関連ノート
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