HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → HCID 21072945, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 21073110 | HCID 21073110 | — |
| Reactant | 2-Ethylbutanedioyl dichloride | HCID 21864608 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Product | HCID 21072945 | HCID 21072945 | 95.7% |
Reaction Steps
A mixture of tert-butyl 3-[5-chloro-2-(3,4-dichlorobenzylamino)phenoxy]benzylcarbamate (2.79 g, 5.5 mmols), ethylsuccinyl chloride (1.2 ml, 8.3 mmols), 4-dimethylaminopyridine (1.01 g, 8.3 mmols) and tetrahydrofuran (30 ml) was stirred at room temperature for 1 hour, and then at 60° C. for 3 hours. The reaction mixture was poured into water, and extracted with ethyl acetate. The extract was washed with brine, and then dried with anhydrous magnesium sulfate. This was concentrated under reduced pressure, and the residue was purified through silica gel column chromatography to give an oil of ethyl N-[2-[3-(tert-butoxycarbonylaminomethyl)phenoxy]-4-chlorophenyl]-N-(3,4-dichlorobenzyl)succinamate (3.34 g, 95.7%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07160887B1 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-3a30f2cdd6914f7cb2a3311d95dfc0b7 |
| Source note | uspto-grants-2007_01 |