HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium Hydroxide → Glycine, N-[(2-oxo-2H-1-benzopyran-3-yl)carbonyl]-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Coumarine 3-carboxamide, N-metoxycarbonylmethyl- | HCID 599285 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Glycine, N-[(2-oxo-2H-1-benzopyran-3-yl)carbonyl]- | HCID 12191927 | — |
Reaction Steps
A solution of coumarin-3-carbonylamino-acetic acid methyl ester (312 mg, 1.19 mmol), in THF (12 ml) under Ar atmosphere, at 0° C. (ice bath), a solution of LiOH in H2O (0.2 M) was added dropwise. The reaction mixture was stirred vigorously at room temperature until total conversion was observed by TLC (2 hours). The solution was partially concentrated and Et2O was added (10 ml). The organic layer was washed with NaHCO3 (10 ml, sat) and the combined aquous layers were acidified with 10% KHSO4 (pH=3-4) and extracted with ether (3×20 ml). The organic layer was concentrated at reduced pressure to afford 8G9C1 (280 mg, 95%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07348310B2 |
| Source dataset | uspto-grants-2008_03 |
| ORD ID | ord-644b9337ca70425dae1f7c7632258036 |
| Source note | uspto-grants-2008_03 |