Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2240063Generated: November 1, 2026

Hydrochloric Acid → 1-[3-(2-Chloro-ethoxy)-5-methoxy-2-nitro-phenylmethanesulfonyl]-naphthalene

https://huagongshe.com/reaction/2240063

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-((Chloromethyl)sulfonyl)naphthaleneHCID 11736608—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant2-(2-Chloroethoxy)-4-methoxy-1-nitrobenzeneHCID 68679874—
SolventTetrahydrofuranHCID 8028—
Product1-[3-(2-Chloro-ethoxy)-5-methoxy-2-nitro-phenylmethanesulfonyl]-naphthaleneHCID 6868043176.7%

Reaction Steps

A mixture of 2-(2-chloro-ethoxy)-4-methoxy-1-nitrobenzene (1.4 g, 6 mmoles) and 1-chloromethane-sulfonyl-naphthalene (1.4 g, 6 mmoles) was stirred in THF (50 mL) at −78° C., in a round bottom flask under nitrogen. A solution of 1M potassium t-butoxide was added dropwise (18 mL, 18 mmoles) over a half an hour period. Temperature was allowed to rise to −40° C., and the reaction mixture was stirred at this temperature for 4 hours. The reaction mixture was poured into cold 2N HCl, extracted with EtOAc, dried over Na2SO4, and concentrated under vacuum. Compound was recrystallized from CH2Cl2/hexane to afford the title compound as an off-white solid (2 g, 4.6 mmoles).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723329B2
Source datasetuspto-grants-2010_05
ORD IDord-b60aaf61883c4f1d8a6c08145678cd78
Source noteuspto-grants-2010_05