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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1810200Generated: November 2, 2026

Benzenesulfonyl chloride → HCID 58107388, compound

https://huagongshe.com/reaction/1810200

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 44771633HCID 44771633—
SolventDichloromethaneHCID 6344—
ProductHCID 58107388HCID 5810738856.2%

Reaction Steps

To a well-agitated suspension of sodium hydroxide (0.81 g, 20.2 mmol) in methylene chloride (10 mL) is added 2,2-dimethyl-1-(1,3,4,9-tetrahydro-pyrido[3,4-b]indol-2-yl)-propan-1-one (2.3 g, 8.98 mmol). The reaction mixture is stirred for 15 min, and then benzenesulfonyl chloride (1.89 g, 10.7 mmol) is added. The solution is stirred at room temperature for 1 h. The reaction is diluted with methylene chloride, washed with water then a saturated sodium chloride solution, dried with sodium sulfate and concentrated in vacuo. Purification by silica gel chromatography (50% ethyl acetate-hexane) provides 2.0 g (56.2%) of the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362063B2
Source datasetuspto-grants-2013_01
ORD IDord-1d003302aee9426280498cff741a51ff
Source noteuspto-grants-2013_01