HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 53814510, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 53743745 | HCID 53743745 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 53814510 | HCID 53814510 | — |
Reaction Steps
6-(4-Chlorosulfonylphenyl)-3-diazo-2,4-hexanedione (2.0 g, 6.4 mmol) obtained in Example 3, (3) was stirred in triethylamine (1.5 ml) and ethanol (5 ml) for 16 h at room temperature, then the mixture was poured into H2O and extracted thrice with chloroform. The organic extract was washed with H2O, dried over anhydrous MgSO4 and evaporated under reduced pressure. The residue was chromatographed on silica gel (Wako Gel C-200) with chloroform as eluent to give the title compound as a pale yellow viscous oil; yield: 550 mg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05250669 |
| Source dataset | uspto-grants-1993_10 |
| ORD ID | ord-917ee152be424e97ac99d45181bb44f3 |
| Source note | uspto-grants-1993_10 |