HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → (R)-4-Amino-6-(4-heptyloxy-phenyl)-4-methyl-hex-1-yn-3-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (R)-5-Ethynyl-4-[2-(4-heptyloxy-phenyl)-ethyl]-4-methyl-oxazolidin-2-one | HCID 86615288 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (R)-4-Amino-6-(4-heptyloxy-phenyl)-4-methyl-hex-1-yn-3-ol | HCID 86615289 | — |
Reaction Steps
To a stirred solution of (R)-5-Ethynyl-4-[2-(4-heptyloxy-phenyl)-ethyl]-4-methyl-oxazolidin-2-one in ethanol (1 ml) is added NaOH (1 ml, 1M aqueous solution). The mixture is heated at reflux temperature for 20 hours. The reaction mixture is then poured onto a biphasic mixture of AcOEt and NaHCO3 (saturated aqueous solution). The aqueous phase is extracted with AcOEt (3 times). The combined organic layers are dried (Na2SO4) and concentrated under reduced pressure. The product is purified by RP-HPLC (ZORBAX Extend C-18) eluting with 5%→95% CH3CN in H2O (+0.1% TFA) to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07928093B2 |
| Source dataset | uspto-grants-2011_04 |
| ORD ID | ord-c09e78a6c8de4d79ba4aaf5df008d1c1 |
| Source note | uspto-grants-2011_04 |