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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 706355Generated: October 29, 2026

Cinnamaldehyde → HCID 10456106, compound

https://huagongshe.com/reaction/706355

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCinnamaldehydeHCID 637511—
ReactantHCID 86605018HCID 86605018—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10456106HCID 1045610695%

Reaction Steps

1-(2-Chloropyridin-4-yl)carbonylspiro[indoline-3,4′-piperidine]trifluoroacetic acid salt (0.44 g) and trans-cinnamaldehyde (0.29 g) were suspended in tetrahydrofuran (8 ml) and ethanol (6 ml). Borane-pyridine complex (0.26 ml) was added and the reaction stirred vigorously overnight at room temperature. The mixture was evaporated and partitioned between dichloromethane and water. The organics were dried over anhydrous magnesium sulfate and evaporated in vacuo. Flash chromatography [SiO2; ethyl acetate-hexane-triethylamine (25:75:1), increasing polarity to (50:50:1)] yielded 0.42 g (94%) of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174987B2
Source datasetuspto-grants-2015_11
ORD IDord-6b2c3c616d5046d88dac6a5f436f22f1
Source noteuspto-grants-2015_11