HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butanol → HCID 86753233, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | HCID 18945165 | HCID 18945165 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86753233 | HCID 86753233 | — |
Reaction Steps
A mixture of methyl 3-(2-carboxyethyl)-5-(pyrrol-1-yl)benzoate (1.5 g), diphenylphosphoryl azide (1.25 ml) and triethylamine (0.8 ml) in tert-butyl alcohol (20 ml) was refluxed for 7 hours. After being cooled to room temperature, the reaction mixture was poured into a mixture of ethyl acetate and water. The organic layer was successively washed with 1N-hydrochloric acid, water and brine and dried over magnesium sulfate. The solvent was evaporated in vacuo and the residue was purified by column chromatography on silica gel eluting with chloroform. The eluted fractions containing the desired product were collected and evaporated in vacuo to give methyl 3-(2-tert-butoxycarbonylaminoethyl-5-(pyrrol-1-yl)benzoate (0.89 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05824691 |
| Source dataset | uspto-grants-1998_10 |
| ORD ID | ord-4b5878e6a797463f839eabba0397be70 |
| Source note | uspto-grants-1998_10 |