Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2075957Generated: November 2, 2026

Methanol → 2-[5-Benzyloxy-4-methoxy-2-(5-methyl-[1,2,4]oxadiazol-3-yl) phenyl]N-tert-butyl-2-hydroxyacetamide

https://huagongshe.com/reaction/2075957

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantEthyl AcetateHCID 8857—
ReactantSodium HydroxideHCID 14798—
ReactantAcetic Acid [5-benzyloxy-4-methoxy-2-(5-methyl-[1,2,4]-oxadiazol-3-yl)phenyl]tert-butylcarbamoylmethyl EsterHCID 86647228—
SolventWaterHCID 962—
Product2-[5-Benzyloxy-4-methoxy-2-(5-methyl-[1,2,4]oxadiazol-3-yl) phenyl]N-tert-butyl-2-hydroxyacetamideHCID 67096487100.4%

Reaction Steps

A mixture of acetic acid [5-benzyloxy-4-methoxy-2-(5-methyl-[1,2,4]oxadiazol-3-yl)phenyl]-tert-butylcarbamoyl methyl ester (Reference example 12-1) (604 mg), a 5 mol/L aqueous solution of sodium hydroxide (1 mL) and methanol (8 mL) was stirred at room temperature for 1.5 hours. Ethyl acetate and water were added to the mixture. The separated organic layer was washed with water, an aqueous solution of sodium bicarbonate successively, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to give the title compound (552 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07923462B2
Source datasetuspto-grants-2011_04
ORD IDord-3dfc5ee8a49b47fd9b2d43567bbce7e7
Source noteuspto-grants-2011_04