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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1430467Generated: October 27, 2026

Ethanol → Ethyl 2-(2-chloro-4-fluoro-5-nitrophenyl)acetate

https://huagongshe.com/reaction/1430467

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSulfuryl chlorideHCID 24648—
Reactant2-(2-Chloro-4-fluoro-5-nitrophenyl)acetic acidHCID 68983333—
ProductEthyl 2-(2-chloro-4-fluoro-5-nitrophenyl)acetateHCID 6898495098%

Reaction Steps

A 0° C. solution of 2-(2-chloro-4-fluoro-5-nitrophenyl)acetic acid (20.5 g, 88 mmol) in EtOH (150 mL) was treated with sulfuryl dichloride (21 g, 0.17 mol), then heated to reflux for 1 h. The reaction mixture was concentrated under reduced pressure and treated with satd. Na2CO3 to pH 7-8. The resultant mixture was extracted with EtOAc (3×) and the combined organic layers were washed with brine, dried (MgSO4) and concentrated to give ethyl 2-(2-chloro-4-fluoro-5-nitrophenyl)acetate (22.5 g, 98% yield). 1H NMR (400 Hz, DMSO-d6): δ 8.32 (d, J=8.0 Hz, 1H), 7.91 (d, J=11.2 Hz, 1H), 4.09 (q, J=7.2 Hz, 2H), 3.92 (s, 2H), 1.17 (t, J=7.2 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940756B2
Source datasetuspto-grants-2015_01
ORD IDord-455861b73e244fe9b0621bece7ae58e7
Source noteuspto-grants-2015_01