HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → HCID 45091960, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | (S)-2-(Boc-Amino)-N-methoxy-n-methylbutyramide | HCID 10422029 | — |
| Reactant | Acetone cardice | HCID 18522661 | — |
| Reactant | HCID 178467906 | HCID 178467906 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 45091960 | HCID 45091960 | — |
Reaction Steps
A solution of tert-butyl{(1S)-1-[methoxy(methyl)carbamoyl]propyl}carbamate (15.0 g) in tetrahydrofuran (150 mL) was cooled using dry ice/acetone under a nitrogen atmosphere, and 1.0 mol/L-methyllithium/diethyl ether solution (300 mL) was added. The mixture was stirred at the same temperature for 4 hr, saturated aqueous ammonium chloride solution (300 mL) was added to the reaction solution, and the mixture was extracted with ethyl acetate. The obtained organic layer was washed with saturated aqueous ammonium chloride solution and saturated brine, dried over anhydrous magnesium sulfate, and concentration under reduced pressure to give the title compound as a colorless oil (yield: 12.75 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07834051B2 |
| Source dataset | uspto-grants-2010_11 |
| ORD ID | ord-719dbfe999d448aeb74b5d69697ecbdf |
| Source note | uspto-grants-2010_11 |