Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 618273Generated: October 30, 2026

Sulfuric Acid → 1-methansulfonyl-1H-indol-6-ol

https://huagongshe.com/reaction/618273

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantSodium BicarbonateHCID 516892—
ReactantN-methanesulfonyl-6-aminoindoleHCID 18789618—
ReactantSodium NitriteHCID 23668193—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product1-methansulfonyl-1H-indol-6-olHCID 18789668—

Reaction Steps

N-methansulfonyl-6-amino indole (2.10 g, 10.0 mmol), prepared as described in Forbes, et al., J. Med. Chem. (1996) 39:4968, was suspended in 40 ml of water, then cooled in an ice bath. Concentrated sulfuric acid (3 ml) was added slowly dropwise. The mixture was warmed to room temperature for 5 min then cooled back down to 0° C. A solution of NaNO2 (Mallinckrodt, 0.76 g, 11.0 mmol) in 10 ml of water was added slowly and the resultant foam was treated with 10 ml of ethanol. The mixture was added in portions to a boiling solution of CUSO4 (J. T. Baker, 16.0 g, 0.1 mol) in 75 ml of water. After 15 min, the mixture was cooled. The brown solid which had formed was broken up with a glass stirring rod. NaHCO3 was added to neutralize the reaction and the product was extracted with ethyl acetate (2×100 ml). The extracts were dried (anhydrous MgSO4) and concentrated to give 1-methansulfonyl-1H-indol-6-ol (1.62 g), a brown oil which was used with out purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05952362
Source datasetuspto-grants-1999_09
ORD IDord-7cb961e407044738b5a94c57d144e346
Source noteuspto-grants-1999_09