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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1922540Generated: October 31, 2026

Phenylboronic Acid → HCID 59730978, compound

https://huagongshe.com/reaction/1922540

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylboronic AcidHCID 66827—
ReactantTri-o-tolylphosphineHCID 80271—
ReactantBarium hydroxide, octahydrateHCID 17749109—
ReactantHCID 59730973HCID 59730973—
Catalystpalladium(II) acetateHCID 167845—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 59730978HCID 5973097826.2%

Reaction Steps

Next, to a mixture of 2-(3-bromophenyl)-N-(7-hydroxy-5,6,7,8-tetrahydronaphthalen-1-yl)acetamide (50.0 mg, 0.139 mmol), phenyl boronic acid (25.4 mg, 0.208 mmol), tri-o-tolylphosphine (8.45 mg, 0.028 mmol), and barium hydroxide octa-hydrate (65.7 mg, 0.208 mmol) in 12 mL of ethylene glycol dimethyl ether was added ethanol (4 ml,), water (4 mL), and palladium(II) acetate (3.12 mg, 0.014 mmol). The mixture was stirred vigorously under argon and was heated to reflux. After cooled to room temperature, water was added and the product was extracted with ethylacetate. The organic layer was washed with water then brine, dried over MgSO4, filtered, and concentrated under reduced pressure to obtain 2-biphenyl-3-yl-N-(7-hydroxy-5,6,7,8-tetrahydronaphthalen-1-yl)acetamide (13.0 mg, 26% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173841B2
Source datasetuspto-grants-2012_05
ORD IDord-ec3edacd66764160a13387832fdcac2e
Source noteuspto-grants-2012_05