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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1766115Generated: October 26, 2026

Chlorosulfonic acid → Ethyl 2-(4-(chlorosulfonyl)-2-ethylphenoxy)acetate

https://huagongshe.com/reaction/1766115

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfonic acidHCID 24638—
ReactantEthyl (2-ethylphenoxy)acetateHCID 21986411—
ProductEthyl 2-(4-(chlorosulfonyl)-2-ethylphenoxy)acetateHCID 2198634370%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a 250 ml round-bottom flask containing chlorosulfonic acid (30 ml) cooled to 0° C. was added ethyl (2-ethylphenoxy)acetate (7.2 g, 34.6 mmoles) dropwise. Once the addition was complete the ice-bath was removed and the reaction was allowed to warm to room temperature at which the reaction was stirred for 3 hours. The reaction was then slowly added to ice and, once the excess chlorosulfonic acid was quenched, the mixture was diluted with CH2Cl2 (200 ml). The phases were separated and the aqueous fraction was washed with CH2Cl2 twice. The combined organic fractions were dried over Na2SO4 and filtered and concentrated in vacuo to yield 7.2 g (70%) of crude product. The crude product was used with no purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07229998B2
Source datasetuspto-grants-2007_06
ORD IDord-2e0e51a231b6470393197a0a42a9a039
Source noteuspto-grants-2007_06