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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231367Generated: October 31, 2026

HCID 70379608, compound → HCID 86743225, compound

https://huagongshe.com/reaction/231367

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 70379608HCID 70379608—
ReactantHCID 70379838HCID 70379838—
SolventNitric AcidHCID 944—
SolventSulfuric AcidHCID 1118—
ProductHCID 86743225HCID 86743225—

Reaction Steps

6 g (0.025 moles) of 2-nitrotetrafluoroethoxybenzene or 4-nitrotetrafluoroethoxybenzene are dissolved in 20 ml concentrated sulfuric acid (density, d=1.84 g/ml) and nitrated at 5°-10° C. with a mixture of 1.2 ml nitric acid (d=1.5 g/ml) and 5 ml sulfuric acid (d=1.84 g/ml). After the addition of the nitrating acid, the aforesaid preparation is allowed to heat at room temperature. The preparation, after being left to stand overnight, is then poured onto ice water. The precipitated oil is separated by means of decanting and the aqueous phase is extracted three times with 50 ml ether. The ether extracts and the oil are then combined, washed with sodium bicarbonate solution so as to be acid-free and dried over calcium chloride. After distilling the solvent, 6.6 g (93% of the theoretical yield) dinitro compound (from the 2-nitrotetrafluoroethoxybenzene) or 6.7 g (94% of the theoretical yield) dinitrotetrafluoroethoxybenzene (from the 4-nitrotetrafluoroethoxybenzene) is obtained. The dinitro compound was further processed directly in the following step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04845294
Source datasetuspto-grants-1989_07
ORD IDord-4e1f3003f31c439db1fbe2eca3c72602
Source noteuspto-grants-1989_07