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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1776583Generated: October 31, 2026

HCID 86679535, compound → HCID 86679536, compound

https://huagongshe.com/reaction/1776583

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86679535HCID 86679535—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductHCID 86679536HCID 8667953690%

Reaction Steps

A mixture of 2-(benzyloxy)-2-oxoethyl 2-(tert-butoxycarbonyloxy)-5-(N-(cyclopropylmethyl)methylsulfonamido)benzoate (0.288 g, 0.540 mmol) and 10% w/w Pd/C (0.030 g, 0.028 mmol) in MeOH (20 ml) and EtOAc (5 ml) was hydrogenated at 20 psi for 3 hours. The catalyst was filtered off and the solvent was removed affording 2-(2-(tert-butoxycarbonyloxy)-5-(N-(cyclopropylmethyl)-methylsulfonamido)benzoyloxy)-acetic acid (0.215 g, 0.485 mmol, 90% yield). This product was used without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09265768B2
Source datasetuspto-grants-2016_02
ORD IDord-c12bf9593d6a47dea4d9e346561fab9c
Source noteuspto-grants-2016_02