HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → HCID 70818548, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Ethyl oxoacetate | HCID 70211 | — |
| Reactant | HCID 70818685 | HCID 70818685 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 70818548 | HCID 70818548 | 29% |
Reaction Steps
Butyl lithium (1.6M, 930 μL, 1.5 mmol) was added at −78° C. to a solution of 4-(3,4-dihydro-2H-1-benzopyran-6-yl)-2-phenyl-1,3-thiazole (9c) (330 mg, 1.12 mmol) in anhydrous tetrahydrofuran (10 mL). After 20 minutes, ethyl glyoxylate 50% in toluene (400 μL, 2 mmol) was added at −78° C. and the mixture was stirred for 2 hours, hydrolyzed with water and concentrated in vacuo. The residue was diluted with ethyl acetate (20 mL) and the organic layer was washed with water (10 mL), brine (10 mL), dried over sodium sulfate, filtered and evaporated under reduced pressure. The residue was purified by flash chromatography on silica gel (cyclohexane/ethyl acetate 80/20) to afford the desired alcohol (9d) as a white solid (130 mg, 0.33 mmol, 29%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09238026B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-6770edb496f349e685037ffe1de23958 |
| Source note | uspto-grants-2016_01 |