Benzoic Acid → HCID 57280076, compound
Reaction equation
[CH2:1]([O:5][C@@H:6]([CH3:12])[CH2:7][CH2:8][C@@H:9](O)[CH3:10])[CH2:2][CH2:3][CH3:4].[C:13]([OH:21])(=[O:20])[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.N(C(OCC)=O)=NC(OCC)=O>CCOCC>[C:13]([O:21][C@@H:9]([CH2:8][CH2:7][C@@H:6]([O:5][CH2:1][CH2:2][CH2:3][CH3:4])[CH3:12])[CH3:10])(=[O:20])[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1Participants
Procedure
That is, 1.23 g of (2S,5S)-5-butoxy-2-hexanol, 0.86 g of benzoic acid and 2.78 g of triphenylphosphine were dissolved in 25 ml of dry ether. Thereto was dropwise added 2.29 g of diethyl azodicarboxylate (DEAD) at room temperature with stirring. The mixture was stirred for 1 hour at room temperature. The reaction mixture was concentrated under reduced pressure. The residue was separated and purified by silica gel column chromatography (eluting solvent: dichloromethane) to obtain 1.56 g of (2R,5S)-5-butoxy-2-hexyl benzoate as a colorless oily substance. 1.56 g of the product was dissolved in 20 ml of methanol. Thereto was dropwise added 516 ml of a 1 N methanol solution of sodium hydroxide at room temperature with stirring. The mixture was stirred for 8 hours at room temperature. The reaction mixture was mixed with 15 ml of water and stirred for 8 hours. To the resulting reaction mixture was added water. Then, extraction with dichloromethane was effected. The extract was dried and concentrated. The residue was subjected to Kugel-rohr distillation under reduced pressure to obtain 0.57 g of the title compound as a colorless oil.
Workup
- customat room temperature
- stirringThe mixture was stirred for 1 hour at room temperature
- concentrationThe reaction mixture was concentrated under reduced pressure
- customThe residue was separated
- custompurified by silica gel column chromatography (eluting solvent: dichloromethane)
Sources & evidence
- ORD record
- ord-655c5bd3b11e4f348021263437fa7c68
- Source dataset
- uspto-grants-1992_10
- Patent number
- US05152919
Reaction notes
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