HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butanol → HCID 70222659, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | HCID 10694323 | HCID 10694323 | — |
| Catalyst | Cuprous chloride | HCID 62652 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 70222659 | HCID 70222659 | — |
Reaction Steps
A mixture of 1.9 g (9.6 mmols) of N,N′-dicyclohexylcarbodiimide, 1.06 ml (11.2 mmols) of absolute tert.butanol and 0.020 g (0.20 mmol) of copper(I) chloride was stirred for 60 hours at room temperature. Then, 6.6 ml of methylene chloride were added, and the resulting solution was added dropwise to a solution of 0.44 g (1 mmol) of 2-ethyoxy-4-[N-{1-(2-piperidinophenyl)-1-butyl}-aminocarbonylmethyl]-benzoic acid in 15 ml of methylene chloride. After 60 hours' stirring at 20° C., the precipitate which had formed was filtered off, washed with methylene chloride, and the methylene chloride solution was evaporated in vacuo. The evaporation residue was purified by column chromatography on silica gel (chloroform/ethyl acetate=9/1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | USRE037035E1 |
| Source dataset | uspto-grants-2001_01 |
| ORD ID | ord-ae763b5b5ab6477a8f40377cc889797f |
| Source note | uspto-grants-2001_01 |