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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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Boron tribromide → HCID 52951573、化合物

HRID 445860
ノート
印刷プレビュー

反応式

HRID 445860 の反応式
C[O:2][C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][CH:11]=1)[CH2:8][CH:7]([C:12]([O:14][CH3:15])=[O:13])[CH2:6]2.B(Br)(Br)Br>ClCCl>[OH:2][C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][CH:11]=1)[CH2:8][CH:7]([C:12]([O:14][CH3:15])=[O:13])[CH2:6]2
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 2

HCID 25134Boron tribromideHCID 53724337Methyl 5-methoxy-2,3-dihydro-1H-indene-2-carboxylate

生成物 1

HCID 52951573HCID 52951573、化合物

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
0 °C

実験手順

To a solution of methyl 5-methoxy-2,3-dihydro-1h-indene-2-carboxylate (696) (2.35 g, 11.4 mmol) in anhydrous dichloromethane (40 mL) cooled to −78° C. was added boron tribromide (1.5 eq.). The reaction was allowed to stir at −78° C. for 30 minutes, 0° C. for 2 hours, and at room temperature overnight. The reaction mixture was cooled to 0° C. and quenched slowly with methanol. After stirring for 15 minutes a saturated sodium bicarbonate solution was added slowly to the mixture and allowed to stir at 0° C. for 30 minutes. Ethyl acetate was added and the layers were separated. The aqueous layer was extracted with ethyl acetate and the combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo to afford methyl 5-hydroxy-2,3-dihydro-1H-indene-2-carboxylate (697).

後処理

  1. customat room temperature
  2. customovernight
  3. temperatureThe reaction mixture was cooled to 0° C.
  4. customquenched slowly with methanol
  5. stirringAfter stirring for 15 minutes a saturated sodium bicarbonate solution
  6. additionwas added slowly to the mixture
  7. stirringto stir at 0° C. for 30 minutes
  8. additionEthyl acetate was added
  9. customthe layers were separated
  10. extractionThe aqueous layer was extracted with ethyl acetate
  11. dry with materialthe combined organic layers were dried over sodium sulfate
  12. filtrationfiltered
  13. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-6da10ad337854c7fb87256af472d13ca
出典データセット
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08476308B2

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