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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 873672Generated: October 30, 2026

Benzenesulfonyl chloride → HCID 58107388, compound

https://huagongshe.com/reaction/873672

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 numberUS08975439B2
Source datasetuspto-grants-2015_03
ORD IDord-48e70d57e6784fd380abefd8b9c8d24b
Source noteuspto-grants-2015_03