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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1589698Generated: November 1, 2026

HCID 9865661, compound → HCID 9951222, compound

https://huagongshe.com/reaction/1589698

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 9865661HCID 9865661—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventBenzeneHCID 241—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductHCID 9951222HCID 9951222—

Reaction Steps

24.3 g of 6-acetoxy-2,5,7,8-tetramethyl-2-(4-nitrophenoxymethyl)chroman were dissolved in a mixture of 200 ml of methanol and 20 ml of benzene and reacted for 3 hours under a hydrogen pressure of 45-55 lb/sq. inch (3.1-3.8 bars), using Pearl's hydrogen adding apparatus, in the presence of 7 g of 10% w/w palladium-on-carbon. The palladium-on-carbon was removed by filtration from the reaction mixture and washed with a mixture of 600 ml of acetone and 60 ml of concentrated hydrochloric acid. The filtrate and the washings were combined and the mixture was neutralized with sodium bicarbonate. The solvent was then distilled off, and the crude crystals obtained were dissolved in ethyl acetate. The ethyl acetate solution was washed with water and dried over anhydrous sodium sulfate. The ethyl acetate was then distilled from the extract, and the crude substance obtained was washed with a 1:1 by volume mixture of benzene and cyclohexane, giving the desired 6-acetoxy-2-(4-aminophenoxymethyl)-2,5,7,8-tetramethylchroman, melting at 138°-140° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04572912
Source datasetuspto-grants-1986_02
ORD IDord-0118b5420d0a4cd0ba621e3e1447acae
Source noteuspto-grants-1986_02