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(Diethylamino)sulfur trifluoride → HCID 14612530、化合物

HRID 859893
ノート
印刷プレビュー

反応式

HRID 859893 の反応式
[N:1]([CH2:4][C@@H:5]1[C@@H:9](O)[CH2:8][N:7]([CH2:11][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[CH2:6]1)=[N+:2]=[N-:3].C(N(S(F)(F)[F:24])CC)C.C(=O)([O-])O.[Na+]>ClCCl>[N:1]([CH2:4][C@@H:5]1[C@@H:9]([F:24])[CH2:8][N:7]([CH2:11][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[CH2:6]1)=[N+:2]=[N-:3]
参加物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 123472(Diethylamino)sulfur trifluorideHCID 516892Sodium BicarbonateHCID 86600237HCID 86600237、化合物

生成物 1

HCID 14612530HCID 14612530、化合物

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

実験手順

(3R,4R)-3-Azidomethyl-1-benzyl-4-hydroxypyrrolidine (566 mg) was dissolved in dichloromethane (9 mL). While this solution was cooled on an ice bath, diethylaminosulfur trifluoride (0.39 mL) was added dropwise and the mixture was stirred at room temperature for 2 hours. While the reaction vessel was cooled on an ice bath, a saturated aqueous solution of sodium hydrogen carbonate (9 mL) was added, and the mixture was diluted with dichloromethane (15 mL). The dichloromethane layer was collected and the collected dichloromethane layer was washed with a saturated aqueous solution of sodium hydrogen carbonate (10 mL) and then water (10 mL), was dried over anhydrous sodium sulfate, and was concentrated under reduced pressure. The resulting residue was purified on a silica gel column (eluant=hexane:ethyl acetate=4:1). From the first half fraction, 76.7 mg of (3R,4R)-3-azidomethyl-1-benzyl-4-fluoropyrrolidine was obtained as a pale brown oil.

後処理

  1. temperatureWhile this solution was cooled on an ice bath
  2. temperatureWhile the reaction vessel was cooled on an ice bath
  3. customThe dichloromethane layer was collected
  4. washthe collected dichloromethane layer was washed with a saturated aqueous solution of sodium hydrogen carbonate (10 mL)
  5. dry with materialwater (10 mL), was dried over anhydrous sodium sulfate
  6. concentrationwas concentrated under reduced pressure
  7. customThe resulting residue was purified on a silica gel column (eluant=hexane:ethyl acetate=4:1)

出典と根拠

ORDレコード
ord-f4fe28fe8e464c56ba426f2953cdaae8
出典データセット
uspto-grants-2006_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07153851B2

反応ノート

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