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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2203452Generated: October 30, 2026

HCID 89544105, compound → HCID 89544134, compound

https://huagongshe.com/reaction/2203452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 89544105HCID 89544105—
CatalystPalladiumHCID 23938—
SolventEthylacetate methanolHCID 21584119—
ProductHCID 89544134HCID 8954413498%

Reaction Steps

A mixture of 3-benzhydryl-5-(2-(benzyloxy)-5-methylphenyl)benzo[d]oxazol-2(3H)-one (1.0 g, 2.0 mmol) and palladium on activated charcoal (10% w/w, 0.20 g) in ethyl acetate/methanol (1:1 v/v, 20 mL) was stirred under an atmosphere of hydrogen (1 atm) for 16 h. The reaction mixture was filtered through a pad of diatomaceous earth and the pad was washed with ethyl acetate/methanol (1:1 v/v, 20 mL). The filtrate and washes were combined and concentrated in vacuo. The residue was purified by column chromatography eluting with a 20-65% gradient of ethyl acetate in hexanes to afford 3-benzhydryl-5-(2-hydroxy-5-methylphenyl)benzo[d]oxazol-2(3H)-one as a colorless solid in 98% yield (0.80 g): 1H NMR (300 MHz, CDCl3) δ 7.38-7.32 (m, 6H), 7.30-7.24 (m, 5H), 7.17-7.12 (m, 1H), 6.99 (dd, J=8.2, 1.6 Hz, 1H), 6.84 (s, 1H), 6.79-6.73 (m, 2H), 6.51 (s, 1H), 4.68 (s, 1H), 2.24 (s, 3H); MS (ES+) m/z 407.8 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365578B2
Source datasetuspto-grants-2016_06
ORD IDord-ecb1bf5b679d48fdbd92f2b4ed4d862b
Source noteuspto-grants-2016_06