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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1259131Generated: November 2, 2026

Benzaldehyde → HCID 86652349, compound

https://huagongshe.com/reaction/1259131

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantLithium diisopropylamideHCID 2724682—
ReactantHCID 86652350HCID 86652350—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86652349HCID 86652349—

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of 3-bromo-6-chloro-5-methylpicolinonitrile (from the previous step) in THF (0.2 M) was cooled to −78° C. LDA (2N solution, 2 eq) was added dropwise. The reaction was kept stirring at −78° C. for 1 hour, followed by addition of benzaldehyde (1 eq). The reaction was kept stirring at −78° C. for another 30 minutes before allowing it to slowly warm to room temperature. The reaction was quenched with sat. NH4Cl and extracted with EtOAc. Combined organic washes were concentrated. Flash chromatography (silica gel, 20-50% EtOAc in hexanes) afforded the product 3-bromo-6-chloro-5-(2-hydroxy-2-phenylethyl)picolinonitrile as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466167B2
Source datasetuspto-grants-2013_06
ORD IDord-c9ba00acb50a419cb383a31a6eea2bcf
Source noteuspto-grants-2013_06