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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384048Generated: October 30, 2026

N-Phenyl diethanolamine → 2-Methyl-2-(6-(6-phenyl-1,3,6,2-dioxazaborocan-2-yl)pyridin-2-yl)propanenitrile

https://huagongshe.com/reaction/384048

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Phenyl diethanolamineHCID 8416—
ReactantTriisopropyl borateHCID 21531—
Reactant2-(6-Bromopyridin-2-yl)-2-methylpropanenitrileHCID 57969658—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product2-Methyl-2-(6-(6-phenyl-1,3,6,2-dioxazaborocan-2-yl)pyridin-2-yl)propanenitrileHCID 5796963159.1%

Reaction Steps

A stirred solution of 2-(6-bromopyridin-2-yl)-2-methylpropanenitrile (1 g, 4.44 mmol) and triisopropylborate (1.23 ml, 5.33 mmol) in tetrahydrofuran (10 ml) was cooled down to −75° C. A 2.5 M solution of n-BuLi in hexanes (2.31 ml, 5.77 mmol) was added at such a rate that the temperature did not exceed −67° C. After complete addition, the reaction was allowed to warm to room temperature and was stirred at this temperature for 16 hours. After this time, a solution of N-phenyldiethanolamine (805 mg, 4.44 mmol) in THF (8 ml) was added and the resulting mixture was heated at reflux for 4 hours. The mixture was concentrated in vacuo, diluted with isopropanol (18 ml) and refluxed for 1 hour. The reaction mixture was cooled down to room temperature and stirred for 18 hours. The newly formed solid was filtered off and dried under vacuo at 40° C. to afford the title compound as a white solid (880 mg, 59% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367697B2
Source datasetuspto-grants-2013_02
ORD IDord-14e64df879de475e9c112e6ab4fd34be
Source noteuspto-grants-2013_02