HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 131711189, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Boc-Val-osu | HCID 98768 | — |
| Reactant | O-BENZYL-L-THREONINE | HCID 6951054 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 131711189 | HCID 131711189 | — |
Reaction Steps
A suspension of H-Thr(Bzl)-OH (3.0 g, 14.34 mmol) in DMF (60 ml) was mixed with Et3N (2 ml) and Boc-Val-OSu (4.96 g, 15.78 mmol) at 0° C for 2 hours and then at 25° C for 24 hours. Acetic acid was added to about pH 3 and the solvents removed under reduced pressure. The product was extracted into EtOAc, washed with 5% AcOH and water, dried (MgSO4) and evaporated to clear oil which crystallized from EtOAc with petroleum ether to yield 4.9 g (83.1%); mp 132°-135° C; [α]D25 +21.5° (c, 1, CHCl3). Anal. Calcd for C21H32N2O6 (408.49): C, 61.74; H, 7.89; N, 6.85. Found: C, 61.61; H, 7.76; N, 6.80.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04105652 |
| Source dataset | uspto-grants-1978_08 |
| ORD ID | ord-1d4909911b6249fabafaa203ad9671b7 |
| Source note | uspto-grants-1978_08 |