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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903348Generated: October 31, 2026

Trifluoroacetic anhydride → HCID 20468620, compound

https://huagongshe.com/reaction/1903348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantHCID 13259764HCID 13259764—
SolventDiethyl EtherHCID 3283—
ProductHCID 20468620HCID 2046862042.2%

Reaction Steps

Trifluoroacetic anhydride (8.4 g, 0.04 mole) was added portionwise to a solution of 2-hydroxyethyl 5-(2-chloro-4-trifluoromethylphenoxy)-2-nitrobenzoate (7 g, 0.017 mole) and 50 ml of ether. After holding at 30°-35° C. for an hour, the solution was allowed to stand at room temperature overnight. Excess trifluoroacetic anhydride was removed and 300 ml of ether was added. The ethereal solution was washed three times with water, dried over CaSO4 and concentrated to an oil. Kugelrohr distillation afforded 3.6 g of pure 2-(trifluoroacetoxy)ethyl 5-(2-chloro-4-trifluoromethylphenoxy)-2-nitrobenzoate as a gumming material (yield: 42.2%); nmr (CDCl3) δ 4.62 (s, 4H), 7.02-8.19 (m, 6H); ir (CHCl3) 1752, 1803 Cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04435588
Source datasetuspto-grants-1984_03
ORD IDord-2b75958e8b43482f92947efd41d32030
Source noteuspto-grants-1984_03