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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1098655Generated: October 31, 2026

Sodium methanesulfinate → HCID 86643713, compound

https://huagongshe.com/reaction/1098655

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium methanesulfinateHCID 2733271—
ReactantHCID 86643712HCID 86643712—
SolventEthyl AcetateHCID 8857—
SolventHeptaneHCID 8900—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 86643713HCID 86643713—

Reaction Steps

A solution of an appropriately protected ethyl (3-amino-8-bromo-1,2,3,4-tetrahydro-9H-carbazol-9-yl)-acetate derivative of Structure 2c (0.238 mmol), cuprous iodide (204 mg, 1.073 mmol, 4.5 eq.) and sodium methanesulfinate (129 mg, 1.073 mmol, 4.5 eq.) in degassed NMP (5 ml) is heated under inert atmosphere at 140° C. overnight. Then, the mixture is diluted with heptane (5 ml) and AcOEt (5 ml) and filtered over a pad of silica gel with AcOEt as eluent. The solvent is removed in vaccuo and the residue dissolved in AcOEt and H2O. The phases are separated and the aq. phase is extracted twice with AcOEt. The combined org. phases are washed with brine and H2O, dried over Na2SO4 and concentrated in vacuuo to yield the corresponding ethyl (3-amino-8-methanesulfonyl-1,2,3,4-tetrahydro-9H-carbazol-9-yl)-acetate derivative of Structure 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143304B2
Source datasetuspto-grants-2012_03
ORD IDord-dc05b7aeaed04f96b3104bb4e41a7072
Source noteuspto-grants-2012_03