Propylethinylcarbinol → (1-Ethynylbutoxy)acetic Acid Ethyl Ester

HRID 18822

Reaktionsgleichung

Reaktionsgleichung von HRID 18822
[CH:1]#[C:2][CH:3]([OH:7])[CH2:4][CH2:5][CH3:6].[N+](=[CH:10][C:11]([O:13][CH2:14][CH3:15])=[O:12])=[N-]>ClCCl.CCCCCCC.CC(O)=O.CC(O)=O.CC(O)=O.CC(O)=O.[Rh].[Rh]>[CH2:14]([O:13][C:11](=[O:12])[CH2:10][O:7][CH:3]([C:2]#[CH:1])[CH2:4][CH2:5][CH3:6])[CH3:15]

Komponenten

6

Edukt 2

HCID 7746PropylethinylcarbinolHCID 12192Ethyl diazoacetate

Produkt 1

HCID 86140139(1-Ethynylbutoxy)acetic Acid Ethyl EsterAusbeute 54,3 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 423677Acetic acid, rhodium salt (4:2)KatalysatorHCID 6344DichloromethaneLösungsmittelHCID 8900HeptaneLösungsmittel

Versuchsvorschrift

To a solution of 1-hexyn-3-ol (981 mg, 10.0 mmol) in dichloromethane (20 mL) is added rhodium (II) acetate dimer (10 mg) followed by ethyl diazoacetate (1.0 mL, 9.0 mmol). The reaction mixture is stirred at rt for 6 h. The reaction mixture is diluted with heptane, and filtered. The filtrate is evaporated, and the residue purified by chromatography on silica gel: elution with EtOAc:heptane (25:75) gives 900 mg of the product 446. 1H NMR (CDCl3) δ 4.35-4.10 (m, 5 H), 2.43 (s, 1 H), 1.90-1.65 (m, 2 H), 1.65-1.40 (m, 2 H), 1.40-1.20 (m, 3 H), 0.95 (t, 3 H)

Aufarbeitung

  1. filtrationfiltered
  2. customThe filtrate is evaporated
  3. customthe residue purified by chromatography on silica gel
  4. washelution with EtOAc:heptane (25:75)

Quellen und Nachweise

ORD-Eintrag
ord-8bf3d22982394b67b3c5d92fe4440613
Quelldatensatz
uspto-grants-2010_06
Patentnummer
US07741493B2

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