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(Diethylamino)sulfur trifluoride → HCID 14612530、化合物

HRID 2108787
ノート
印刷プレビュー

反応式

HRID 2108787 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 chilled in an ice water 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 chilled in an ice water bath, a saturated aqueous solution of sodium bicarbonate (9 mL) was added and the mixture was diluted with dichloromethane (15 mL). The dichloromethane layer was separated, washed sequentially with a saturated aqueous solution of sodium bicarbonate (10 mL) and water (10 mL), dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluant: hexane: ethyl acetate=4:1). The first half fraction yielded (3R,4R)-3-azidomethyl-1-benzyl-4-fluoropyrrolidine as a pale brown oil (76.7 mg).

後処理

  1. temperatureWhile this solution was chilled in an ice water bath
  2. temperatureWhile the reaction vessel was chilled in an ice water bath
  3. customThe dichloromethane layer was separated
  4. washwashed sequentially with a saturated aqueous solution of sodium bicarbonate (10 mL) and water (10 mL)
  5. dry with materialdried over anhydrous sodium sulfate
  6. concentrationconcentrated under reduced pressure
  7. customThe resulting residue was purified by silica gel column chromatography (eluant: hexane: ethyl acetate=4:1)

出典と根拠

ORDレコード
ord-f595ee5e5e1944e4a04b80c63523d5fc
出典データセット
uspto-grants-2009_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07514451B2

反応ノート

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