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Vinyl propanoate → 3-Cyanocyclohex-3-en-1-yl propanoate

HRID 1852467
ノート
印刷プレビュー

反応式

HRID 1852467 の反応式
[OH:1][CH:2]1[CH2:7][C:6]([C:8]#[N:9])=[CH:5][CH2:4][CH2:3]1.[C:10](OC=C)(=[O:13])[CH2:11][CH3:12]>CC(OC)(C)C>[C:10]([O:1][CH:2]1[CH2:3][CH2:4][CH:5]=[C:6]([C:8]#[N:9])[CH2:7]1)(=[O:13])[CH2:11][CH3:12]
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 7750Vinyl propanoateHCID 601605645-Hydroxycyclohex-1-ene-1-carbonitrile

生成物 1

HCID 867310083-Cyanocyclohex-3-en-1-yl propanoate

試薬・触媒・溶媒 1

HCID 15413tert-Butyl methyl ether溶媒

実験手順

To a 2 L flask containing racemic 5-hydroxycyclohex-1-ene-1-carbonitrile (151 g, 1.22 mol), vinyl propionate (147 g, 1.47 mol), and MTBE (1.5 L) was added the enzyme AMANO Lipase PS from Burlholderiacepacia (20 g, Sigma-Aldrich). The mixture was stirred at ambient temperature for 48 hours. The mixture was filtered through celite and rinsed with MTBE. The filtrate was concentrated in vacuo to remove both solvent and unreacted vinyl propionate. The residue was diluted with brine (1.5 L) and extracted with hexanes (1000 mL+600 mL×3 respectively). The combined organics was washed with H2O (400 mL×5), then dried over anhydrous Na2SO4, and concentrated in vacuo to afford the title compound, which was used without further purification.

後処理

  1. additionwas added the enzyme AMANO Lipase PS from Burlholderiacepacia (20 g, Sigma-Aldrich)
  2. filtrationThe mixture was filtered through celite
  3. washrinsed with MTBE
  4. concentrationThe filtrate was concentrated in vacuo
  5. customto remove both solvent and unreacted vinyl propionate
  6. additionThe residue was diluted with brine (1.5 L)
  7. extractionextracted with hexanes (1000 mL+600 mL×3 respectively)
  8. washThe combined organics was washed with H2O (400 mL×5)
  9. dry with materialdried over anhydrous Na2SO4
  10. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-033dd34259d8426994284001470f1a53
出典データセット
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08962608B2

反応ノート

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