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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 862348Generated: October 31, 2026

Sulfamic Acid → HCID 10208859, compound

https://huagongshe.com/reaction/862348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfamic AcidHCID 5987—
ReactantTriacetoxyperiodinaneHCID 159087—
ReactantHCID 18427642HCID 18427642—
ReactantSodium ChloriteHCID 23668197—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 10208859HCID 1020885917.3%

Reaction Steps

(1RS, 2SR, 3RS)-3-[2-(3-Hydroxyprop-1-yloxy)-4-methoxyphenyl]-1-(3,4-methylenedioxyphenyl)-5-(prop-1-yloxy)indane-2-carboxylic acid (0.07 g, 0.13 mmol) was dissolved in dry dichloromethane (0.5 ml) and Dess-Martin periodinane (0.07 g, 0.17 mmol) added in dry dichloromethane (1 ml). After 2h. the product was partitioned between ether and saturated aqueous sodium carbonate solution containing sodium thiosulfate. The ether extract was washed with water then brine, dried (MgSO4 anhydrous), filtered and evaporated to give an oil which was used without purification. The crude product was dissolved in t-butanol (5 ml) and to this was added a solution of sodium chlorite (1 8 mg, 0.2 mmol) and sulfamic acid (21 mg, 0.22 mmol) in water (1.5 ml). After 1 h. stirring at ambient temperature the product was extracted into ethyl acetate. The organic layer was washed with water then brine then dried (MgSO4 anhyd.) filtered and evaporated to give an oil. The product was purified by column chromatography on silica-gel (eluant: ethyl acetate/hexane/3% acetic acid) to give 12 mg of free acid which was converted to its bis-dicyclohexylamine salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05716984
Source datasetuspto-grants-1998_02
ORD IDord-2fecf8fa81cf4fe983890aa082f03edc
Source noteuspto-grants-1998_02