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Hydrochloric Acid → 1-Propioloylpyrrolidine

HRID 2191080
ノート
印刷プレビュー

反応式

HRID 2191080 の反応式
[NH:1]1[CH2:5][CH2:4][CH2:3][CH2:2]1.C[C:7]#[C:8][C:9]([O-])=[O:10].Cl>O.CO.C(Cl)Cl>[C:9]([N:1]1[CH2:5][CH2:4][CH2:3][CH2:2]1)(=[O:10])[C:8]#[CH:7]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 3

HCID 313Hydrochloric AcidHCID 31268PyrrolidineHCID 6994510HCID 6994510、化合物

生成物 1

HCID 3378061-Propioloylpyrrolidine収率 98%

試薬・触媒・溶媒 3

HCID 887Methanol溶媒HCID 962Water溶媒HCID 6344
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
Dichloromethane
溶媒

実験手順

To a stirred solution of pyrrolidine (4.2 mL, 50.0 mmol) in water (25 mL) and MeOH (35 mL) at −50° C. was added methylpropiolate (4.5 mL, 50.0 mmol) dropwise. The reaction mixture was stirred at this temperature for 5 h then diluted with DCM (200 mL). 2M aqueous HCl (200 mL) was added and the layers were separated. The aqueous layer was extracted with DCM (2×100 mL). The combined organic layers were washed with aqueous sat. NaHCO3 (200 mL), water (200 mL), then brine (200 mL), dried (Na2SO4), filtered and concentrated in vacuo to give the title compound (6.0 g, 98%) as a white solid that was used without further purification. δH (CDCl3) 3.68 (2H, t, J 6.8 Hz), 3.50 (2H, t, J 6.3 Hz), 3.04 (1H, s), 2.01-1.90 (4H, m).

後処理

  1. customthe layers were separated
  2. extractionThe aqueous layer was extracted with DCM (2×100 mL)
  3. washThe combined organic layers were washed with aqueous sat. NaHCO3 (200 mL), water (200 mL)
  4. dry with materialbrine (200 mL), dried (Na2SO4)
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-ecc256d397de4f7da88291afcae7638b
出典データセット
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08324204B2

反応ノート

読み込み中…