HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → HCID 11120630, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | tert-Butyl Formate | HCID 61207 | — |
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | HCID 68715991 | HCID 68715991 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 11120630 | HCID 11120630 | — |
Reaction Steps
To a solution of lithium borohydride in tetrahydrofuran (2M, 1.14 ml, 2.28 mmol) was added slowly at 0° C. a solution of (R)-3-benzenesulfonyl-2-tert-butoxycarbonylamino-propionic acid methyl ester (0.52 g, 1.51 mmol) in tetrahydrofuran (3 ml). After stirring at room temperature for 2.5 hours methanol was added (0.5 ml). The mixture was partitioned between ethyl acetate and saturated ammoniumchloride solution. The combined organic layers were dried (MgSO4), filtered and evaporated. The residue was purified by column chromatography (SiO2, heptane/EtOAc=1:1 to yield a white solid, (0.292 g, 61%); MS (ISP): 316.0 ((M+H)+/); 216.1 ((M+H—BOC)+.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08604061B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-eea36d475f404851be4e34bc0dfe0080 |
| Source note | uspto-grants-2013_12 |