HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dicyclohexylcarbodiimide → (S)-4-[4'-(2''-methylbutylcarbonyloxy)phenyl]-1-benzyloxybenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | (S)-3-methyl-pentanoic acid | HCID 642230 | — |
| Reactant | 4-(4-Benzyloxyphenyl)phenol | HCID 15268847 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (S)-4-[4'-(2''-methylbutylcarbonyloxy)phenyl]-1-benzyloxybenzene | HCID 20645782 | 92.2% |
Reaction Steps
{circle around (1)}: A mixture comprising 2.8 g of 4-(4′-benzyloxyphenyl)phenol, 1.2 g of (S)-2-methylbutylcarboxylic acid, 3.09 g of DCC and 15 g of dichloromethane was stirred at room temperature for 30 minutes. Then, a catalytic amount of 4-N,N-dimethylaminopyridine was added to the mixture, and the mixture was further stirred at room temperature for 12 hours. After finishing the reaction, insoluble substances were filtered off, followed by distilling off dichloromethane from the filtrate. The resultant residue was purified by means of silica gel column chromatography, whereby 3.5 g of (S)-4-[4′-(2″-methylbutylcarbonyloxy)phenyl]-1-benzyloxybenzene was obtained in the form of a colorless crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06217793B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-f7f6de8ed2ec4105a7df70badad5e3ab |
| Source note | uspto-grants-2001_04 |