Sodium Hydroxide → HCID 12788636, compound
Reaction equation
C([O:3][C:4]([CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH:12]1[N:16]([CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)[C:15](=[O:28])[NH:14][C:13]1=[O:29])=[O:5])C.[OH-].[Na+]>>[C:4]([CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH:12]1[N:16]([CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)[C:15](=[O:28])[NH:14][C:13]1=[O:29])([OH:5])=[O:3]Participants
3
Procedure
The foregoing ester (4.0 g) was hydrolysed by treatment with dilute sodium hydroxide solution and the product was purified by chromatography on silica gel, to give 5-(6-carboxyhexyl)-1-(5-phenylpentyl)hydantoin crystallising from ethyl acetate-light petroleum (b.p. 60°-80° C.) in colourless prismatic needles, m.p. 90°-92° C.
Workup
- customthe product was purified by chromatography on silica gel
Sources & evidence
- ORD record
- ord-b673a5fd89c0480fa8afbd4246462eaf
- Source dataset
- uspto-grants-1980_05
- Patent number
- US04204068
Reaction notes
Loading…