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Ammonium Chloride → 3-AZIDO-1,1,1-TRIFLUOROPROPAN-2-OL

HRID 1926659
ノート
印刷プレビュー

反応式

HRID 1926659 の反応式
[F:1][C:2]([F:7])([F:6])[CH:3]1[O:5][CH2:4]1.[Cl-].[NH4+].[N-:10]=[N+:11]=[N-:12].[Na+]>C(O)C>[N:10]([CH2:4][CH:3]([OH:5])[C:2]([F:7])([F:6])[F:1])=[N+:11]=[N-:12]
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 25517Ammonium ChlorideHCID 33557Sodium AzideHCID 5207692-(Trifluoromethyl)oxirane

生成物 1

HCID 108773493-AZIDO-1,1,1-TRIFLUOROPROPAN-2-OL

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

To a stirred solution of 1,1,1-trifluoro-2,3-epoxypropane (2.0 g, 18 mmol) in 70% ethanol (20 mL) was added ammonium chloride (1.9 g, 36 mmol) followed by sodium azide (2.3 g, 36 mmol). The reaction mixture was stirred at room temperature. After 6 h, the reaction mixture was partitioned between water (100 mL) and diethyl ether (100 mL). The organic layer was washed with additional water (100 mL). The first aqueous layer was back-extracted with diethyl ether (100 mL). The combined organic layers were dried over magnesium sulfate, filtered and concentrated to give 3-azido-1,1,1-trifluoropropan-2-ol as a crude oil. 1H NMR (600 MHz, DMSO-D6) 4.14 (m, 1H); 3.58-3.49 (m, 2H); 2.58 (d, 1H).

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. customthe reaction mixture was partitioned between water (100 mL) and diethyl ether (100 mL)
  2. washThe organic layer was washed with additional water (100 mL)
  3. extractionThe first aqueous layer was back-extracted with diethyl ether (100 mL)
  4. dry with materialThe combined organic layers were dried over magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated

出典と根拠

ORDレコード
ord-672260838ec04f779ef82eed9edd236c
出典データセット
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08183245B2

反応ノート

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