Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2104262Generated: October 26, 2026

Chlorosulfonic acid → 6-Acetylamino-3-methoxy-5,6,7,8-tetrahydronaphthalene-2-sulfonyl chloride

https://huagongshe.com/reaction/2104262

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfonic acidHCID 24638—
Reactant7-Methoxy-2-acetamido-tetralinHCID 10013697—
Product6-Acetylamino-3-methoxy-5,6,7,8-tetrahydronaphthalene-2-sulfonyl chlorideHCID 86601315—

Reaction Conditions

Temperature-10 °C

Reaction Steps

To chlorosulfonic acid (15 mL), cooled to −10° C. was added N-(7-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl)-acetamide (1.44 g; 6.6 mmol). The reaction mixture was stirred at −10° C. for 15 min and quenched carefully by pouring over ice-water. The aqueous phase was extracted with CH2Cl2 (3×), the organic extracts combined, dried over Na2SO4, filtered and evaporated under reduced pressure to yield 6-acetylamino-3-methoxy-5,6,7,8-tetrahydronaphthalene-2-sulfonyl chloride as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576238B2
Source datasetuspto-grants-2009_08
ORD IDord-98e8c080765c4f459cc7d30a76be4397
Source noteuspto-grants-2009_08