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Tert-Butyl nitrite → HCID 59542484、化合物

HRID 1809090
ノート
印刷プレビュー

反応式

HRID 1809090 の反応式
[CH2:1]([O:3][C:4]([C:6]1[CH:10]=[C:9]([CH:11]2[CH2:16][CH2:15][CH2:14][CH2:13][CH2:12]2)[S:8][C:7]=1N)=[O:5])[CH3:2].N(OC(C)(C)C)=O.[Cl-].[NH4+]>[Cu](Cl)Cl>[CH2:1]([O:3][C:4]([C:6]1[CH:10]=[C:9]([CH:11]2[CH2:16][CH2:15][CH2:14][CH2:13][CH2:12]2)[S:8][CH:7]=1)=[O:5])[CH3:2]
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 10906Tert-Butyl nitriteHCID 25517Ammonium ChlorideHCID 59542544HCID 59542544、化合物

生成物 1

HCID 59542484HCID 59542484、化合物収率 76.7%

試薬・触媒・溶媒 1

HCID 24014Cupric Chloride触媒

実験手順

2-Amino-5-(cyclohexyl)-thiophene-3-carboxylic acid ethyl ester (1.79 g, 7 mmol) was added to a mixture of t-butyl nitrite (10.5 mmol) and copper (II) chloride (7 mmol) in IMS (100 mL). The reaction mixture was stirred for 30 minutes then saturated aqueous ammonium chloride (7 mL) was added and the resulting solution stirred overnight. The solvent was then evaporated under vacuum and the residue partitioned between ethyl acetate and water. The organic solution was separated and dried with magnesium sulphate, filtered and the solvent evaporated to give the title compound as an orange oil (1.28 g). 1H NMR δ (ppm) (CHCl3-d): 7.9 (s, 1H), 7.2 (s, 1H), 4.3 (q, 2H), 2.8 (m, 1H), 2.1 (m, 2H), 1.9 (m, 2H), 1.7-1.2 (m, 9H).

後処理

  1. stirringthe resulting solution stirred overnight
  2. customThe solvent was then evaporated under vacuum
  3. customthe residue partitioned between ethyl acetate and water
  4. customThe organic solution was separated
  5. dry with materialdried with magnesium sulphate
  6. filtrationfiltered
  7. customthe solvent evaporated

出典と根拠

ORDレコード
ord-2e5ecd95568840c599f1b4502724cd7f
出典データセット
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08362008B2

反応ノート

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