HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1681152Generated: November 3, 2026
Benzyl Bromide → Acetyl 9-benzyl-1,2,3,4-tetrahydro-beta-carboline
https://huagongshe.com/reaction/1681152
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Acetyl-1,2,3,4-tetrahydro-beta-carboline | HCID 19807225 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Acetyl 9-benzyl-1,2,3,4-tetrahydro-beta-carboline | HCID 54345929 | — |
Reaction Steps
2 acetyl-9 benzyl-1,2,3,4-tetrahydro-β-carboline was prepared as follows: Under a nitrogen atmosphere, 8.0 mmol of 2 acetyl-1,2,3,4-tetrahydro-β-carboline (1.71 was dissolved in 4Q mL dry dimethylformamide (DMF). The solution was stirred over ice, and NaH (2 g) was added under N2. The suspension was stirred for 1 hour, and then benzylbromide (9.2 mmol, 1.56 was slowly to the cooled suspension. After a further 2 hours of stirring at ambient temperature, the mixture was filtered and the filtrate added to 320 mL 0.1 N HCl. Crude 2-acetyl- 9-benzyl-1,2,3,4-tetrahydro-β-carboline separated as an oil. The oil was collected by centrifugation, washed with water, and dried over anhydrous MgSO:. The product was purified by standard chromatographic procedures using a 60:40 mixture of ether:hexane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05169852 |
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| Source dataset | uspto-grants-1992_12 |
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| ORD ID | ord-f3d60b7a64564e9d91b2ea65bf6dcd9d |
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| Source note | uspto-grants-1992_12 |
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