Menthol → (-)-Menthyl acetoacetate
Reaction equation
[CH:1]1([CH3:11])[CH2:6][CH2:5][CH:4]([CH:7]([CH3:9])[CH3:8])[CH:3]([OH:10])[CH2:2]1.[C:12](OCCCC)(=[O:17])[CH2:13][C:14]([CH3:16])=[O:15]>C1(C)C=CC=CC=1>[C:12]([O:10][C@H:3]1[C@H:4]([CH:7]([CH3:8])[CH3:9])[CH2:5][CH2:6][C@@H:1]([CH3:11])[CH2:2]1)(=[O:17])[CH2:13][C:14]([CH3:16])=[O:15]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 23 °C
Procedure
A solution of (-)-menthol (23.0 g, 147 mmol, 1 equiv) and 1-butyl acetoacetate (20.0 ml, 121 mmol, 0.80 equiv) in toluene (50 mL) was heated at reflux for 12 h, then was cooled to 23° C. Volatiles were removed in vacuo and toluene (20 mL) and 1-butyl acetoacetate (12.2 mL, 73.5 mmol, 0.50 equiv) were added to the residue. The resulting solution was heated at reflux for 12 h, then was cooled to 23° C. The cooled reaction mixture was concentrated in vacuo and the residue was purified by distillation under reduced pressure (bp 90° C., 30 mmHg) to afford (1R,3R,4S)-p-menth-3-yl acetoacetate (1) as a low-melting solid (33.3 g, 94%). ##STR14##
Workup
- temperatureat reflux for 12 h
- additionwere added to the residue
- temperatureThe resulting solution was heated
- temperatureat reflux for 12 h
- temperaturewas cooled to 23° C
- customThe cooled reaction mixture
- concentrationwas concentrated in vacuo
- distillationthe residue was purified by distillation under reduced pressure (bp 90° C., 30 mmHg)
Sources & evidence
- ORD record
- ord-49e109631b9549f6b649f9cc75d04290
- Source dataset
- uspto-grants-1998_06
- Patent number
- US05763451
Reaction notes
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