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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014394Generated: October 31, 2026

Water → HCID 59441628, compound

https://huagongshe.com/reaction/1014394

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium NitriteHCID 23668193—
ReactantHCID 67317722HCID 67317722—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 59441628HCID 5944162870%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of (2R)-1-acetyl-2-methyl-5-(methyloxy)-2,3-dihydro-1H-indole (100 mg, 0.487 mmol)—see (Arp, Forrest O.; Fu, Gregory C. Kinetic Resolutions of Indolines by a Nonenzymatic Acylation Catalyst. Journal of the American Chemical Society (2006), 128(44), 14264-14265.)—in TFA (2 mL) at 0° C. was treated with sodium nitrite (33.6 mg, 0.487 mmol). The resulting red solution was stirred at 0° C. for 1 h. H2O (20 mL) was added, the resulting slurry was filtered and the solids were washed with water to afford (2R)-1-acetyl-2-methyl-5-(methyloxy)-6-nitro-2,3-dihydro-1H-indole as a yellow solid (85 mg, 70%). 1H NMR (400 MHz, DMSO-d8) δ ppm 1.22 (d, J=6.41 Hz, 3H), 2.22 (s, 3H), 2.76 (d, J=17.21 Hz, 1H), 3.45 (dd, J=17.12, 8.88 Hz, 1H), 3.89 (s, 3H), 4.59-4.74 (m, 1H), 7.35 (s, 1H), 8.40 (s, 1H); ESIMS (M+H)+=251.00.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981903B2
Source datasetuspto-grants-2011_07
ORD IDord-2daf02d2dd5e404780252c717318d3bf
Source noteuspto-grants-2011_07