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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Dichloromethane → HCID 86700905、化合物

HRID 625120
ノート
印刷プレビュー

反応式

HRID 625120 の反応式
[Cl:1][C:2]1[CH:9]=[C:8]([O:10]C)[C:5]([CH:6]=[O:7])=[C:4]([O:12][CH3:13])[CH:3]=1.C(Cl)Cl.B(Br)(Br)Br>>[Cl:1][C:2]1[CH:3]=[C:4]([O:12][CH3:13])[C:5]([CH:6]=[O:7])=[C:8]([OH:10])[CH:9]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 6344DichloromethaneHCID 25134Boron tribromideHCID 867009044-Chloro-2,6-dimethoxybenzaldehyde

生成物 1

HCID 86700905HCID 86700905、化合物収率 99%

反応条件

温度
-78 °C

実験手順

A stirred solution of 4-chloro-2,6-dimethoxybenzaldehyde (Example 37A, 1.95 g, 9.72 mmol) in DCM (20 mL, 311 mmol) at −78° C. was slowly added boron tribromide (9.72 mL, 9.72 mmol). The reaction mixture was stirred at −78° C. for 10 minutes then warmed to r.t. and stirred for 1 hour while monitoring reaction progress by LCMS. Once all s.m. had been consumed, the reaction was quenched with water and extracted with DCM. The organic phase was washed with brine, dried (MgSO4), filtered and concentrated to dryness to give the title material (1.79 g, 9.59 mmol, 99% yield) as a purple solid. LC (Method B): 2.199 min. LCMS (APCI) calcd for C8H8ClO3 [M+H]+ m/z 187.02, found 187.0. 1H NMR (CDCl3, 400 MHz) δ ppm: 11.89 (s, 1H), 10.20 (s, 1H), 6.75 (t, J=2.0 Hz, 1H), 6.66 (m, 1H), 3.91 (s, 1H).

後処理

  1. customat −78° C.
  2. temperaturethen warmed to r.t.
  3. stirringstirred for 1 hour
  4. customreaction progress by LCMS
  5. customhad been consumed
  6. customthe reaction was quenched with water
  7. extractionextracted with DCM
  8. washThe organic phase was washed with brine
  9. dry with materialdried (MgSO4)
  10. filtrationfiltered
  11. concentrationconcentrated to dryness

出典と根拠

ORDレコード
ord-813a75e4add842199c8a3735eb80a421
出典データセット
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09303065B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート