HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → HCID 13744912, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-Carbomethoxy-7-mercapto-4-oxo-4H-1-benzopyran | HCID 13744911 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 13744912 | HCID 13744912 | — |
Reaction Steps
The ester from Step 4 (3.0 g) in suspension in methanol (20 ml) and water (40 ml) at 0° was stirred vigorously during the portionwise addition of NaBH4 (1.8 g). The mixture was stirred for 2 hours at 5°. Acetone (1 ml) was added followed by acidification with 1N HCl and extraction with methanolchloroform (1:9, 3×50 ml). The combined extracts were dried (Na2SO4), reduced to dryness in vacuo and the residue was recrystallized from methanolethyl acetate to provide the title compound, m.p. 139°-140°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04761425 |
| Source dataset | uspto-grants-1988_08 |
| ORD ID | ord-65ac2b1ed89d401b9f8e14a7a24b9b35 |
| Source note | uspto-grants-1988_08 |