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Carbon tetrabromide → HCID 23064812、化合物

HRID 735403
ノート
印刷プレビュー

反応式

HRID 735403 の反応式
Br[C:2]([Br:5])(Br)Br.[CH:6]12[O:14][CH:9]([CH:10](CO)[CH2:11]1)[CH:8]=[CH:7]2.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>C(Cl)Cl>[CH:9]12[O:14][CH:6]([CH:11]([CH2:2][Br:5])[CH2:10]1)[CH:7]=[CH:8]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

5

反応物 3

HCID 11205Carbon tetrabromideHCID 11776TriphenylphosphineHCID 2650927-Oxabicyclo[2.2.1]hept-5-en-2-ylmethanol

生成物 1

HCID 23064812HCID 23064812、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

Tetrabromomethane (1.161 g, 3.50 mmol) was added to a solution of 7-oxanorborn-2-en-5-ylmethanol (0.305 g, 2.50 mmol, from Example 2) in CH2Cl2 (12.5 ml). The solution was cooled to 0° C. and admixed with triphenylphosphine (1.836 g, 7 mmol). The reaction mixture was allowed to warm to room temperature and stirred for 12 h. The solvent was removed under reduced pressure and the remaining solid was taken up in cyclohexane. The crude product was purified by flash chromatography (using a 98:2 mixture of cyclohexane and ethyl acetate). 0.3 g (59% of theory) of the pure product were obtained. The product was stored under cool conditions with the exclusion of light.

後処理

  1. temperatureto warm to room temperature
  2. customThe solvent was removed under reduced pressure
  3. customThe crude product was purified by flash chromatography (
  4. additiona 98:2 mixture of cyclohexane and ethyl acetate)
  5. custom0.3 g (59% of theory) of the pure product were obtained

出典と根拠

ORDレコード
ord-afc0d1d530544a1a8b3b9d59f999295f
出典データセット
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07592498B2

反応ノート

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