HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → HCID 14329880, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-[4-(3-bromopropoxy)-2-hydroxy-3-propylphenyl]ethanone | HCID 2775221 | — |
| Reactant | 6-Hydroxy-2-methyl-3,4-dihydro-2H-1-benzopyran-2-carboxylic acid | HCID 18996544 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 14329880 | HCID 14329880 | 68.9% |
Reaction Steps
The procedure of Example 7 was employed to alkylate 0.9 g of the ethyl ester of racemic-3,4-dihydro-6-hydroxy-2-methyl-2H-1-benzopyran-2-carboxylic acid with 4'-(3-bromopropoxy)-2'-hydroxy-3'-n-propylacetophenone (1.5 g), using sodium hydride (12.16 mmole), and sodium iodide (10 mmoles), in N,N-dimethylformamide. After saponification with lithium hydroxide monohydrate (1.5 g), the crude acid product was purified by chromatography on silica gel. There was obtained 1.16 g (68.9%) of racemic-6-[3-(4-acetyl-3-hydroxy-2-propylphenoxy)propoxy]-3,4-dihydro-2-methyl-2H-1-benzopyran-2-carboxylic acid as an off-white solid mp 108°-110.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04785017 |
| Source dataset | uspto-grants-1988_11 |
| ORD ID | ord-97c8162cb1f54c67aa41d776a9503b24 |
| Source note | uspto-grants-1988_11 |