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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 270147Generated: October 26, 2026

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

https://huagongshe.com/reaction/270147

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 250ml round-bottom flask containing chlorosulfonic acid (30ml) cooled to 0° C. was added ethyl (2-ethylphenoxy)acetate (7.2g, 34.6mmoles) 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 3hours. The reaction was then slowly added to ice and, once the excess chlorosulfonic acid was quenched, the mixture was diluted with CH2Cl2(200ml). The phases were separated and the aqueous fraction washed with CH2Cl2twice. The combined organic fractions were dried over Na2SO4and filtered and concentrated in vacuo to yield 7.2g (70%) of crude product. The crude product was used with no purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07449468B2
Source datasetuspto-grants-2008_11
ORD IDord-3f77c5b4fc1248f6a579fbef01fdec08
Source noteuspto-grants-2008_11