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(Diethylamino)sulfur trifluoride → 1-benzhydryl-3-fluoroazetidine

HRID 2201668
ノート
印刷プレビュー

反応式

HRID 2201668 の反応式
CCN(S(F)(F)[F:7])CC.[CH:10]([N:23]1[CH2:26][CH:25](O)[CH2:24]1)([C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1>C(Cl)Cl>[CH:10]([N:23]1[CH2:26][CH:25]([F:7])[CH2:24]1)([C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1
参加物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 123472(Diethylamino)sulfur trifluorideHCID 3304481-(Diphenylmethyl)azetidin-3-ol

生成物 1

HCID 73305071-benzhydryl-3-fluoroazetidine収率 30.3%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

DAST (26.46 g, 0.164 mol) was added to a solution of Compound 19-2 (13.1 g, 0.0547 mol) in dry DCM (200 mL) at 0° C. The reaction mixture was stirred at room temperature overnight. The end of the reaction was monitored with TLC (petroleum ether/ethyl acetate=5:1). The reaction mixture was poured into ice water, extracted with DCM, washed with saturated brine, dried over anhydrous Na2SO4, and the organic layer was concentrated under reduced pressure, the resulting crude product was purified by column chromatography (petroleum ether/ethyl acetate=150:1) to give Compound 19-3 (4.0 g, 30% yield) as a white solid.

後処理

  1. extractionextracted with DCM
  2. washwashed with saturated brine
  3. dry with materialdried over anhydrous Na2SO4
  4. concentrationthe organic layer was concentrated under reduced pressure
  5. customthe resulting crude product was purified by column chromatography (petroleum ether/ethyl acetate=150:1)

出典と根拠

ORDレコード
ord-39f0b24062904d6dbb3215b0fd35dbcb
出典データセット
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09365499B2

反応ノート

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