Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantAcetyl-1,2,3,4-tetrahydro-beta-carbolineHCID 19807225—
SolventDimethylformamideHCID 6228—
ProductAcetyl 9-benzyl-1,2,3,4-tetrahydro-beta-carbolineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05169852
Source datasetuspto-grants-1992_12
ORD IDord-f3d60b7a64564e9d91b2ea65bf6dcd9d
Source noteuspto-grants-1992_12