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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1741416Generated: November 2, 2026

Acetic Anhydride → 1-[N-formyl-N-[(4,5-diphenyloxazol-2-yl)methyl]amino]-2,3-dihydro-4-methoxy-1H-indene

https://huagongshe.com/reaction/1741416

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant1-(4,5-diphenyloxazol-2-yl)methylamino-2,3-dihydro-4-methoxy-1H-indeneHCID 18367313—
SolventFormic AcidHCID 284—
Product1-[N-formyl-N-[(4,5-diphenyloxazol-2-yl)methyl]amino]-2,3-dihydro-4-methoxy-1H-indeneHCID 18367423—

Reaction Steps

To a solution of 1-(4,5-diphenyloxazol-2-yl)methylamino-2,3-dihydro-4-methoxy-1H-indene (0.13 g) in formic acid (5 ml) was added acetic anhydride (1 ml) at 0° C. After being stirred for 5 hours at room temperature, the solvent was evaporated in vacuo. The residue was partitioned between ethyl acetate and 1N hydrochloric acid. The organic layer was washed with water, sat. NaHCO3, and brine. The dried solvent was evaporated in vacuo and the residue was purified by chromatography on silica gel to give 1-[N-formyl-N-[(4,5-diphenyloxazol-2-yl)methyl]amino]-2,3-dihydro-4-methoxy-1H-indene (0.12 g). MS (m/z): 425 (M+ +1) NMR (CDCl3, δ): 8.52 (0.25H, s), 8.43 (0.75H, s), 7.60-7.40 (4H, m), 7.38-7.24 (6H, m), 7.18-6.95 (1H, m), 6.78-6.55 (2H, m), 6.18 (0.25H, m), 5.28 (0.75H, m), 4.72 (0.75H, d, J=16.2 Hz), 4.51 (0.75H, d, J=16.2 Hz), 4.12 (0.5H, m), 3.79 (2.25H, s), 3.72 (0.75H, s), 3.20-2.94 (1H, m), 2.92-2.66 (1H, m), 2.62-2.38 (1H, m), 2.35-2.05 (1H, m)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05972965
Source datasetuspto-grants-1999_10
ORD IDord-ce0b4e390ada4dd5911696f442ad7b7f
Source noteuspto-grants-1999_10