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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 551039Generated: October 27, 2026

Nitric Acid → tert-Butyl [3-nitro-1-(phenylsulfonyl)-1H-indol-4-yl]acetate

https://huagongshe.com/reaction/551039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
Reactanttert-Butyl [1-(phenylsulfonyl)-1H-indol-4-yl]acetateHCID 57426198—
SolventAcetic AnhydrideHCID 7918—
Producttert-Butyl [3-nitro-1-(phenylsulfonyl)-1H-indol-4-yl]acetateHCID 57426199—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To acetic anhydride (5 mL) at 0° C. was added 90% nitric acid (0.183 mL, 3.90 mmol) and the resulting mixture was aged for 10 min, then added dropwise to a solution of tert-butyl [1-(phenylsulfonyl)-1H-indol-4-yl]acetate from Step B (1.00 g, 2.69 mmol) in acetic anhydride (5 mL) at −78° C. The reaction mixture was stirred at −78° C. for 6 h, then aged at −20° C. for 16 b, then quenched with H2O and extracted with EtOAc (2×10 mL). The combined organic extracts were dried over Na2SO4, filtered, and concentrated in vacuo. The crude product was purified by silica gel chromatography, eluting with a gradient of hexane:EtOAc—100:0 to 70:30, to give the title compound. MS: m/z=361 (M−C4H7).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947677B2
Source datasetuspto-grants-2011_05
ORD IDord-e3e1da012faa4439bf7ffa6ab47e6c43
Source noteuspto-grants-2011_05