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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 717077Generated: October 30, 2026

4-Cyanobenzaldehyde → HCID 123820452, compound

https://huagongshe.com/reaction/717077

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-CyanobenzaldehydeHCID 66042—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantN,N-dimethylformamide methanolHCID 21901440—
ReactantHCID 131734155HCID 131734155—
SolventAcetic AcidHCID 176—
ProductHCID 123820452HCID 12382045287.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of 4-formylbenzonitrile (68 mg, 0.51 mmol) and 3-(tert-Butyl-diphenyl-silanyloxy)-3-methyl-azetidine hydrochloride (188 mg, 0.51 mmol) in 1:1 MeOH/DMF (26 mL) was added acetic acid (catalytic). The reaction mixture was stirred under N2 at 0° C. for 1 h. Sodium cyanoborohydride (1M in THF, 0.6 mL, 0.57 mmol) was added and the reaction mixture stirred at RT, under N2 for 18 h. The reaction mixture was concentrated in vacuo, the residue suspended in H2O (10 mL), washed with CH2Cl2 (2×10 mL) and the solution passed through a phase separation cartridge. The combined organic layers were concentrated in vacuo and the crude residue purified by silica gel chromatography eluting with 100% isohexane and increasing the polarity 100% EtOAc to afford 4-[3-(tert-butyl-diphenyl-silanyloxy)-3-methyl-azetidin-1-ylmethyl]-benzonitrile as a colourless oil (196 mg, 86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193689B2
Source datasetuspto-grants-2015_11
ORD IDord-12781841910b462dba066ba7975c83f4
Source noteuspto-grants-2015_11