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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 5,6,7,8-Tetrahydro-2-methylquinoline | HCID 12229420 | — |
| Product | 8-Benzylidene-2-methyl-5,6,7,8-tetrahydro-quinoline | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07276522B2 |
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| Source dataset | uspto-grants-2007_10 |
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| ORD ID | ord-e4548eb584f642a481f7eb5a4c793f73 |
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| Source note | uspto-grants-2007_10 |
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