HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 19105562, compound → HCID 19105565, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 19105562 | HCID 19105562 | — |
| Reactant | HCID 19105566 | HCID 19105566 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium sulfide (PdS) | HCID 82926 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 19105565 | HCID 19105565 | — |
Reaction Steps
A solution of 500 mg (1.9 mmol) of 2,4,4-trimethyl-6-bromo-(4H)-1-benzothiopyran (Compound 50) in 5 ml of ethyl acetate was treated with 500 mg of 10% palladium sulfide on carbon and then shaken under an atmosphere (30 psi) of hydrogen in a Parr apparatus for 24 hours. The mixture was filtered through celite and the solvent was removed in-vacuo. The residue was purified by flash chromatography (silica; hexanes) to give the title compound as a colorless oil. PMR (CDCl3): & 1.21 (3H, s), 1.33 (3H, d, J=6.6Hz), 1.36 (3H, s), 1.64-1.89 (2H, m), 3.37-3.50 (1H, m), 7.10 (1H, dd, J=8.4 Hz, 2.1Hz), 7.19 (1H, d, 8.4 Hz), 7.20 (1H, d, 2.1 Hz)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05162546 |
| Source dataset | uspto-grants-1992_11 |
| ORD ID | ord-99b03c0332214dbdafece52046d652df |
| Source note | uspto-grants-1992_11 |