HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 59775207, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 59775184 | HCID 59775184 | — |
| Reactant | HCID 59775197 | HCID 59775197 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 59775207 | HCID 59775207 | — |
Reaction Steps
To a solution of (R)-4-((S)-4-benzyl-2-oxooxazolidin-3-yl)-3-(4-fluoro-3-methylphenoxy)-4-oxobutanal (35 mg, 0.091 mmol) in 3 mL DCE was added 3-(4-Fluoro-3-methylphenyl)-N-methylpropan-1-amine (22 mg, 0.12 mmol) followed by NaBH(OAc)3 (29.5 mg, 0.14 mmol) and AcOH (7.2 mg, 0.12 mmol) at room temperature. The mixture was stirred for 8 h at the room temperature. The reaction was quenched by pouring into 10 mL 5% aqueous NaOH and diluted with ethyl acetate. The mixture was extracted with more ethyl acetate (3×15 mL) and the combined organic layers washed with brine (2×10 mL) and dried over Na2SO4. The solvent was removed under reduced pressure and the crude product used directly in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07879911B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-5c287d79792a4b28972e9e3f9e4cc607 |
| Source note | uspto-grants-2011_02 |