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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 408737Generated: October 30, 2026

Dimethylformamide → HCID 66937089, compound

https://huagongshe.com/reaction/408737

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTrimethyl orthoformateHCID 9005—
ReactantSodium DithioniteHCID 24489—
Reactant5-Chloro-2-nitro-4-(trifluoromethoxy)anilineHCID 26596607—
SolventAcetic AcidHCID 176—
ProductHCID 66937089HCID 6693708979.1%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 5-chloro-2-nitro-4-trifluoromethoxy-phenylamine (2.00 g, 7.80 mmol), sodium dithionite (7.06 g, 40.5 mmol), trimethyl orthoformate (23.1 mL, 210 mmol), DMF (23 mL), and acetic acid (4.0 mL) was heated in a sealed tube for 15 h at 100° C. The reaction mixture was cooled to 23° C. and partitioned between EtOAc (100 mL) and saturated aq. NaHCO3 (100 mL). The organic layer was collected and the aqueous layer was extracted with EtOAc (2×80 mL). The combined organic layers were dried, filtered, and concentrated under reduced pressure. The residue was purified (FCC) (0-15% MeOH/DCM) to yield the titled compound (1.46 g, 78%). MS (ESI/CI): mass calcd. for C8H4ClF3N2O, 236.0; m/z found, 237.0 [M+H]+. 1H NMR (500 MHz, CDCl3): 8.11 (5, 1H), 7.74 (s, 1H), 7.64 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759345B2
Source datasetuspto-grants-2014_06
ORD IDord-9304c56389a8430e967c24926ffbcba5
Source noteuspto-grants-2014_06