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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266450Generated: October 31, 2026

Potassium Carbonate → HCID 54321425, compound

https://huagongshe.com/reaction/266450

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-Bromo-3,6-dioxaheptaneHCID 123532—
ReactantHCID 54544552HCID 54544552—
SolventMethyl Ethyl KetoneHCID 6569—
ProductHCID 54321425HCID 5432142564%

Reaction Steps

Reaction of 3.03 g (0.01 mol) of 2-benzyl-7-hydroxy-4-methoxybenzisothiazol-3-one-1-oxide (Example 26A) with 2.01 g (0.011 mol) of 2-(2-methoxyethoxy) ethyl bromide in methyl ethyl ketone in the presence of 2 g (0.015 mol) of potassium carbonate afforded 2.58 g (64%) of 2-benzyl-4-methoxy-7-[2-(2-methoxyethoxy) ethoxy]benzisothiazol-3-one-1-oxide, which, on oxidation with 1.1 g (0.0063 mol) of 3-chloroperbenzoic acid in MDC, gave 2-benzyl-4-methoxy-7-[2-(2-methoxyethoxy)-ethoxy]saccharin. Debenzylation of 0.25 g (0.0006 mol) of the product with 0.13 g (0.0021 mol) of ammonium formate in methanol in the presence of 0.25 g of 10% palladium-on-charcoal gave 0.21 g (100%) of the ammonium salt of 4-methoxy-7-[2-(2-methoxyethoxy)ethoxy]saccharin. Reaction of 1.4 g (0.004 mol) of the ammonium salt with 0.63 g (0.004 mol) of chloromethyl phenyl sulfide in DMF afforded 2-phenylthio-methyl-4 -methoxy-7-[2-(2-methoxyethoxy) ethoxy]saccharin, which, on reaction with sulfuryl chloride in MDC, afforded 0.53 g (35%) of 2-chloromethyl-4-methoxy-7-[2-(2-methoxyethoxy) ethoxy]saccharin.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05650422
Source datasetuspto-grants-1997_07
ORD IDord-e50a6e8c5a2843a0ba062ed2ddaa9449
Source noteuspto-grants-1997_07