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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1646810Generated: November 2, 2026

Benzyl 7-(3,5,6-trimethyl-1,4-benzoquinon-2-yl)-7-phenylheptanoylglycinate → HCID 14031665, compound

https://huagongshe.com/reaction/1646810

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl 7-(3,5,6-trimethyl-1,4-benzoquinon-2-yl)-7-phenylheptanoylglycinateHCID 19088032—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 14031665HCID 1403166598.5%

Reaction Steps

Benzyl 7-(3,5,6-trimethyl-1,4-benzoquinon-2-yl)-7-phenylheptanoylglycinate (0.78 g) in ethanol (8 ml) was hydrogenated in the presence of 5% palladium-charcoal (0.08 g) at room temperature. After the reaction was completed, the catalyst was removed by filtration. The solution was treated with ferric chloride (0.51 g) in water (5 ml) at room temperature for 20 min. with stirring. The reaction mixture was worked up in the usual manner. The product was recrystallized from ethylacetate to give 7-(3,5,6-trimethyl-1,4-benzoquinon-2-yl)-7-phenylheptanoylglycine (0.63 g, 98%), mp 162°-164° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05180742
Source datasetuspto-grants-1993_01
ORD IDord-e84773d755c244f29661cafbdf442def
Source noteuspto-grants-1993_01