Ethanol → HCID 7035705, compound
Reaction equation
[CH2:1](O)[CH3:2].S(=O)(=O)(O)O.[C:9]([NH:17][C@H:18]([C:22]([OH:24])=[O:23])[CH:19]([CH3:21])[CH3:20])(=[O:16])[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1>>[C:9]([NH:17][C@H:18]([C:22]([O:24][CH2:1][CH3:2])=[O:23])[CH:19]([CH3:21])[CH3:20])(=[O:16])[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1Participants
4
Procedure
Dissolve in 100 ml of ethanol 0.045 mol (10 g) of N-benzoylvaline obtained in the preceding Step, add 5 ml of concentrated sulphuric acid, then heat at reflux for 24 hours. Evaporate to dryness, take up in ether, wash with water then with a 10% potassium bicarbonate solution, dry, filter and evaporate to dryness. Ethyl N-benzoylvalinate is obtained.
Workup
- customobtained in the preceding Step
- temperatureheat
- temperatureat reflux for 24 hours
- customEvaporate to dryness
- washwash with water
- dry with materialwith a 10% potassium bicarbonate solution, dry
- filtrationfilter
- customevaporate to dryness
Sources & evidence
- ORD record
- ord-f32974852f14475aa494efe18e9dd3d6
- Source dataset
- uspto-grants-1993_10
- Patent number
- US05254548
Reaction notes
Loading…