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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2075956Generated: November 2, 2026

Acetic Acid → Acetic Acid [5-benzyloxy-4-methoxy-2-(5-methyl-[1,2,4]-oxadiazol-3-yl)phenyl]tert-butylcarbamoylmethyl Ester

https://huagongshe.com/reaction/2075956

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantWaterHCID 962—
ReactantAcetonitrileHCID 6342—
ReactantTert-Butyl isocyanideHCID 23577—
Reactant5-Benzyloxy-4-methoxy-2-(5-methyl-[1,2,4]oxadiazol-3-yl)benzaldehydeHCID 59565649—
SolventEthyl AcetateHCID 8857—
ProductAcetic Acid [5-benzyloxy-4-methoxy-2-(5-methyl-[1,2,4]-oxadiazol-3-yl)phenyl]tert-butylcarbamoylmethyl EsterHCID 86647228—

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 5-benzyloxy-4-methoxy-2-(5-methyl-[1,2,4]oxadiazol-3-yl)benzaldehyde (Reference example 15-1) (453 mg), tert-butylisocyanide (465 mg), acetic acid (0.32 mL) and acetonitrile (8 mL) was stirred at 70° C. for 13 hours. After cooling to room temperature, ethyl acetate and water were added to the mixture. The separated organic layer was washed with water, an aqueous solution of sodium bicarbonate, and brine successively, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: 15%-50% ethyl acetate/hexane, gradient elution) to give the title compound (604 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07923462B2
Source datasetuspto-grants-2011_04
ORD IDord-725ea753136447e5be442f51724feb1e
Source noteuspto-grants-2011_04