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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1502632Generated: October 31, 2026

Acetic Acid → HCID 178427610, compound

https://huagongshe.com/reaction/1502632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantMethaneHCID 297—
ReactantEthyl acetate pentaneHCID 22335286—
ReactantHCID 178427611HCID 178427611—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 178427610HCID 178427610100%

Reaction Steps

83.8 mg (0.24 mmol) of N—(N-(2-(benzyloxy)ethyl)carbamimidoyl)-4-methylbenzenesulfonamide were dissolved under nitrogen in MeOH. A few mg of 10% Palladium over activated charcoal were added. 3 vacuo hydrogen flush were done before stirring vigorously the reaction under a H2 atmosphere. After 2 hours, no conversion was found by TLC (eluant AcOEt:pentane 9:1) and approximatively 5 times the amount of starting Palladium over activated charcoal was added. The rection was stirred overnight. The TLC showed the formation of a more polar product unless the reaction was far from being complete. 1 mL of acetic acid was added. One hour after the reaction was complete. The reaction was filtered over celite and the solvent evaporated to afford 62.8 mg (0.24 mmol) of N—(N-(2-hydroxyethyl)carbamimidoyl)-4-methylbenzenesulfonamide as a white solid (yield=100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09211340B2
Source datasetuspto-grants-2015_12
ORD IDord-59a38e2bef664b5aa60fe247c42dbb80
Source noteuspto-grants-2015_12