Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2296412Generated: October 31, 2026

Tetrahydrofuran → HCID 13279412, compound

https://huagongshe.com/reaction/2296412

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
Reactant5-(2-Chloro-4-(trifluoromethyl)phenoxy)-2-nitrobenzoyl chlorideHCID 3017765—
ReactantHCID 13279417HCID 13279417—
SolventDiethyl EtherHCID 3283—
ProductHCID 13279412HCID 13279412—

Reaction Steps

5-(2-Chloro-4-trifluoromethylphenoxy)-2-nitrobenzoyl chloride (4.0 g, 0.0105 mole) was added portionwise to a solution of 8-hydroxy-3,6-dioxaoctyl 2,4-dichlorophenoxyacetate (3.5 g, 0.103 mole), triethylamine (1.2 g, 0.103 mole) and THF (40 ml) over 5 mins. The resulting solution was held at reflux for 3 hrs. After the solvent was stripped off, the residue was taken into 2600 ml of ether, washed two times with NaHCO3 solution and two times with water. The ether solution was then dried over MgSO4 and concentrated to 5.9 g of 8-(2,4-dichlorophenoxyacetoxy)-3,6-dioxaoctyl 5-(2-chloro-4-trifluoromethylphenoxy)-2-nitrobenzoate, a brownish gum; nmr (CDCl3) δ3.30-4.02 (m, 8H), 4.25-4.62 (m, 4H), 4.70 (S, 2H), 6.65-8.24 (m, 9H); ir (CHCl3) 1750, 1770 Cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04429146
Source datasetuspto-grants-1984_01
ORD IDord-7e7e4043b5cb4db48297d068f3ac0a68
Source noteuspto-grants-1984_01