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Pyridine → HCID 119083722、化合物

HRID 2065960
ノート
印刷プレビュー

反応式

HRID 2065960 の反応式
[OH:1][CH:2]([CH3:10])/[CH:3]=[CH:4]/[C:5]([O:7][CH2:8][CH3:9])=[O:6].N1C=CC=CC=1.[Cl:17][CH2:18][C:19](Cl)=[O:20]>CN(C1C=CN=CC=1)C.C1COCC1>[Cl:17][CH2:18][C:19]([O:1][CH:2]([CH3:10])/[CH:3]=[CH:4]/[C:5]([O:7][CH2:8][CH3:9])=[O:6])=[O:20]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 1049PyridineHCID 6577Chloroacetyl chlorideHCID 9989379HCID 9989379、化合物

生成物 1

HCID 119083722HCID 119083722、化合物収率 74%

試薬・触媒・溶媒 2

HCID 142844-(Dimethylamino)pyridine触媒HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
0 °C

実験手順

21 (rac-Ethyl (2E)-4-hydroxypent-2-enoate) (crude, HPLC: ˜94 area %, 9.20 g, 60 mmol), pyridine (9.7 ml, 0.12 mol) and DMAP (1.47 g, 12 mmol) are dissolved in THF (300 ml) and cooled to 0° C. Chloroacetylchloride (9.6 ml, 0.12 mol) in THF (60 ml) is added dropwise under stirring at ≦2° C. over 10 min. The reaction mixture is stirred 40 min at 0° C. The resulting suspension is then poured onto H2O (250 ml) and extracted with tBuOMe (1 l). The organic phase is washed with saturated NaHCO3 (100 ml), 1 M HCl (100 ml), H2O (3×100 ml) and brine (100 ml) successively. The organic phase is dried with Na2SO4 and evaporated under reduced pressure at 40° C. The residue is purified by HPLC (tBuOMe:hexane fraction 5:95) and yields 30 (rac-Ethyl (2E)-4-(chloroacetoxy)pent-2-enoate) (9.81 g, 74%) as a yellowish oil.

後処理

  1. stirringThe reaction mixture is stirred 40 min at 0° C
  2. additionThe resulting suspension is then poured onto H2O (250 ml)
  3. extractionextracted with tBuOMe (1 l)
  4. washThe organic phase is washed with saturated NaHCO3 (100 ml), 1 M HCl (100 ml), H2O (3×100 ml) and brine (100 ml) successively
  5. dry with materialThe organic phase is dried with Na2SO4
  6. customevaporated under reduced pressure at 40° C
  7. customThe residue is purified by HPLC (tBuOMe:hexane fraction 5:95)

出典と根拠

ORDレコード
ord-8b5c13b503684f19987998263988a491
出典データセット
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08288566B2

反応ノート

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