Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 373418Generated: October 27, 2026

HCID 19105562, compound → HCID 19105565, compound

https://huagongshe.com/reaction/373418

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 19105562HCID 19105562—
ReactantHCID 19105566HCID 19105566—
ReactantHCID 178418361HCID 178418361—
CatalystPalladium sulfide (PdS)HCID 82926—
SolventEthyl AcetateHCID 8857—
ProductHCID 19105565HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05162546
Source datasetuspto-grants-1992_11
ORD IDord-99b03c0332214dbdafece52046d652df
Source noteuspto-grants-1992_11