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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2221290Generated: November 1, 2026

Hexane → HCID 69216040, compound

https://huagongshe.com/reaction/2221290

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantN-methyl-2-pyrrolidoneHCID 13387—
ReactantTri-o-tolylphosphineHCID 80271—
Reactant5-Bromonaphthalene-2-carboxylic acidHCID 14960646—
ReactantHCID 178418750HCID 178418750—
CatalystZinc cyanide (Zn(CN)2)HCID 11186—
Catalystpalladium(II) acetateHCID 167845—
ProductHCID 69216040HCID 6921604080%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of Pd(OAc)2 (0.012 g, 0.054 mmol) and tri-o-tolylphosphine (0.073 g, 0.240 mmol) in degassed N-methylpyrrolidone (2 mL) is heated at 60° C. for 30 minutes. A solution of 1.0 M diethylzinc in hexane (0.11 mL, 0.11 mmol) is then added and stirring is continued for additional 30 minutes. To this mixture is added a mixture of 5-bromo-naphthalene-2-carboxylic acid, 1, (0.135 g, 0.536 mmol) and Zn(CN)2 (0.063 g, 0.536 mmol) in degassed N-methylpyrrolidone (2 mL). The resulting mixture is heated at 60° C. for 18 hrs. The reaction mixture is cooled and directly loaded to a prep-HPLC column eluting with CH3CN—H2O (0.1% TFA) to afford 0.085 g (80% yield) of the desired product as a white solid. m.p. 250° C. (dec.). 1H NMR (300 MHz, CDCl3): δ 8.61 (s, 1H), 8.18 (m, 2H), 8.14 (d, J=8.7 Hz, 1H), 7.94 (d, J=7.2 Hz, 1H), 7.54 (t, J=8.4 Hz, 1H). 13C NMR (75 MHz, CDCl3): δ 168.4, 134.9, 134.8, 134.5, 132.4, 131.9, 129.9, 128.5, 125.9, 125.5, 117.5, 110.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07368462B1
Source datasetuspto-grants-2008_05
ORD IDord-234d952bf26c4c22bc790576b55f02e5
Source noteuspto-grants-2008_05