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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2063729Generated: October 31, 2026

Hydrogen Bromide → 9-Benzenesulfonyl-2,3,4,9-tetrahydro-1H-beta-carboline

https://huagongshe.com/reaction/2063729

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantDiethyl EtherHCID 3283—
Reactant9-Benzenesulfonyl-1,3,4,9-tetrahydro-beta-carboline-2-carboxylic acid benzyl esterHCID 10503536—
SolventAcetic AcidHCID 176—
Product9-Benzenesulfonyl-2,3,4,9-tetrahydro-1H-beta-carbolineHCID 44403079—

Reaction Steps

33% hydrogen bromide in glacial acetic acid (20.7 ml) was added to a suspension of the product from stage 2 (4.14 g, 9.27 mmol) in glacial acetic acid (20.7 ml) and the mixture was stirred at room temperature for 1 h. The mixture was poured into diethyl ether (500 ml). The hydrobromide which had precipitated out was filtered off with suction, washed with diethyl ether and dried over potassium hydroxide in a desiccator. Saturated potassium carbonate solution (100 ml) was added to the salt (3.60 g) and the resulting mixture was extracted with methylene chloride (3×25 ml). The combined organic phases were dried with sodium sulfate and concentrated i. vac.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288406B2
Source datasetuspto-grants-2012_10
ORD IDord-de0878fcef444084879e659976b97936
Source noteuspto-grants-2012_10