HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → tert-butyl N-[(2R)-1-oxo-3-phenylpropan-2-yl]carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | Boc-D-phenylalanine methyl ester | HCID 637614 | — |
| Reactant | Potassium sodium tartarate | HCID 9855836 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Toluene methylene chloride | HCID 21877217 | — |
| Product | tert-butyl N-[(2R)-1-oxo-3-phenylpropan-2-yl]carbamate | HCID 7020444 | 89% |
Reaction Steps
To a stirred solution of compound 31c (25.0 g, 90 mmol) in toluene-DCM (4:1, 1000 mL) was added dropwise a solution of DIBAL-H in toluene (1.0 M, 179 mL, 179 mmol) at −78° C. under argon and the mixture was stirred for 1 h at this temperature. Methanol (200 mL) was added immediately to quench the reaction. The reaction mixture was poured into a solution of 200 mL of 20% sodium potassium tartrate (Rochelle salt) and stirred at rt until the two layers separated. The organic layer was concentrated in vacuo and the residue was purified by CC (hexane/EA=2:1) to give compound 31d as a white solid (19.9 g, 89% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08940722B2 |
| Source dataset | uspto-grants-2015_01 |
| ORD ID | ord-b8132475168d47799b0336f2c18ad427 |
| Source note | uspto-grants-2015_01 |