HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 1-[3-(2-Chloro-ethoxy)-5-methoxy-2-nitro-phenylmethanesulfonyl]-naphthalene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1-((Chloromethyl)sulfonyl)naphthalene | HCID 11736608 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | 2-(2-Chloroethoxy)-4-methoxy-1-nitrobenzene | HCID 68679874 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-[3-(2-Chloro-ethoxy)-5-methoxy-2-nitro-phenylmethanesulfonyl]-naphthalene | HCID 68680431 | 76.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07723329B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-b60aaf61883c4f1d8a6c08145678cd78 |
| Source note | uspto-grants-2010_05 |