HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → 2,2,4,4-Tetramethyl-chroman-6-carboxylic acid 4-(tert-butoxycarbonylmethyl)phenyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2,2,4,4-Tetramethyl-3,4-dihydro-2H-1-benzopyran-6-carboxylic acid | HCID 15728709 | — |
| Reactant | Tert-butyl 2-(4-hydroxyphenyl)acetate | HCID 15932404 | — |
| Reactant | t-Butyl-4-hydroxy-phenyl acetate | HCID 23442872 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | Thionyl Chloride | HCID 24386 | — |
| Product | 2,2,4,4-Tetramethyl-chroman-6-carboxylic acid 4-(tert-butoxycarbonylmethyl)phenyl ester | HCID 69548544 | 55% |
Reaction Steps
A solution of 2,2,4,4-tetramethyl chroman-6-carboxylic acid (0.1 g, 0.43 mmol) in thionyl chloride (10 mL) was refluxed for 2 h. The thionyl chloride was evaporated under reduced pressure and the residue was dissolved in 5 mL of dichloromethane and treated with triethyl amine (5 mL) followed by tert-butyl-4-hydroxy phenyl acetate (Reagent E, 0.088 g, 0.427 mmol). After 0.5 h, the reaction mixture was subjected to flash column chromatography over silica gel (230-400 mesh) using 5-10% ethyl acetate in hexane as the eluent to afford the title compound (0.1 g, 55%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06603019B2 |
| Source dataset | uspto-grants-2003_08 |
| ORD ID | ord-e49c6fd32abb41019045f0b4d280d828 |
| Source note | uspto-grants-2003_08 |