HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → (6-Hydroxy-7-t-butyl-5-isopropyl-8-propylchroman-2-yl)acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Trimethyl phosphonoacetate | HCID 80029 | — |
| Reactant | 2-Hydroxy-2-methyl-7-t-butyl-5-isopropyl-8-propyl-chroman-6-yl-acetate | HCID 131718291 | — |
| Product | (6-Hydroxy-7-t-butyl-5-isopropyl-8-propylchroman-2-yl)acetic acid | HCID 54411785 | — |
Reaction Steps
Suspend sodium hydride (47.2 g of 56% in mineral oil, 1.10 mol) in anhydrous tetrahydrofuran (1 L). Place under a nitrogen atmosphere and add, by dropwise addition, trimethyl phosphonoacetate (209.4 g, 1.15 mol). Stir the 25 minutes and add a solution of 2-hydroxy-2-methyl-7-t-butyl-5-isopropyl-8-propyl-chroman-6-yl-acetate (0.5 mol) in tetrahydrofuran (1 L). Stir at room temperature for 18 hour then heat at reflux for 4 hours. Cool, evaporate the solvent in vacuo and purify by chromatography to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05623052 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-6ae32be3706d4970a99758b87e310087 |
| Source note | uspto-grants-1997_04 |