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Boron tribromide → HCID 58415368、化合物

HRID 2075228
ノート
印刷プレビュー

反応式

HRID 2075228 の反応式
B(Br)(Br)Br.[I:5][C:6]1[CH:7]=[C:8]([CH:16]=[CH:17][C:18]=1[O:19]C)[CH2:9][C:10]1[CH:11]=[N:12][CH:13]=[CH:14][CH:15]=1>C(Cl)Cl>[I:5][C:6]1[CH:7]=[C:8]([CH2:9][C:10]2[CH:11]=[N:12][CH:13]=[CH:14][CH:15]=2)[CH:16]=[CH:17][C:18]=1[OH:19]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 25134Boron tribromideHCID 58415249HCID 58415249、化合物

生成物 1

HCID 58415368HCID 58415368、化合物

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

Boron tribromide (11.1 mL, 11.1 mmol, 1M in DCM) was added to a solution of 3-(3-iodo-4-methoxybenzyl)pyridine (720 mg, 2.21 mmol) in DCM (3 mL) at 0° C., and the mixture was stirred for 1 h. The mixture was quenched by the careful addition of water, the layers were separated, and the organic layer was washed with water three times. The combined organic extracts were dried over MgSO4, concentrated in vacuo, and purified by column chromatography to give 2-iodo-4-(pyridin-3-ylmethyl)phenol as a yellow oil. MS (ESI) m/z: Calculated: 311.0; Observed: 312.3 (M++1).

後処理

このページの内容参加物実験手順後処理出典と根拠反応ノート
  1. customThe mixture was quenched by the careful addition of water
  2. customthe layers were separated
  3. washthe organic layer was washed with water three times
  4. dry with materialThe combined organic extracts were dried over MgSO4
  5. concentrationconcentrated in vacuo
  6. custompurified by column chromatography

出典と根拠

ORDレコード
ord-5364a949198f4dab9ecd3f4d4555dc9a
出典データセット
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07919519B2

反応ノート

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