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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1178394Generated: November 2, 2026

Benzaldehyde → 8-Benzylidene-2-methyl-5,6,7,8-tetrahydro-quinoline

https://huagongshe.com/reaction/1178394

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium HydroxideHCID 14798—
Reactant5,6,7,8-Tetrahydro-2-methylquinolineHCID 12229420—
Product8-Benzylidene-2-methyl-5,6,7,8-tetrahydro-quinolineHCID 68892953—

Reaction Steps

A solution of Intermediate 200A1 (27.5 g, 187 mmol), benzaldehyde (18.4 mL, 181 mmol) and acetic anhydride (32.5 mL, 290 mmol) was heated at 155° C. for 4 h. The mixture was cooled to room temperature, mixed with crushed ice, basified with 2M NaOH to pH>8. The aqueous layer was extracted with hexane/ethyl acetate. The pooled organic layers were dried over MgSO4, filtered, evaporated and purified by chromatography on SiO2 to give 8-benzylidene-2-methyl-5,6,7,8-tetrahydro-quinoline (Intermediate 200A2) as the major product. This material was carried onto the next step. Note: 2-styryl-5,6,7,8-tetrahydro-quinoline (removed by chromatography on SiO2 with 1.5% acetone in hexanes) and 8-benzylidene-2-styryl-5,6,7,8-tetrahydro-quinoline were also produced as side products.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07276522B2
Source datasetuspto-grants-2007_10
ORD IDord-e4548eb584f642a481f7eb5a4c793f73
Source noteuspto-grants-2007_10