HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1270596Generated: October 29, 2026
Sodium Hydroxide → 5-(2,6-Dichloro-4-nitro-phenoxy)-2-methoxy-(cyclopropylmethanesulfonyl)-benzene
https://huagongshe.com/reaction/1270596
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Bromomethylcyclopropane | HCID 81503 | — |
| Reactant | 5-(2,6-Dichloro-4-nitro-phenoxy)-2-methoxy-benzenesulfinic acid | HCID 22344879 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-(2,6-Dichloro-4-nitro-phenoxy)-2-methoxy-(cyclopropylmethanesulfonyl)-benzene | HCID 22344875 | 14% |
Reaction Steps
To a solution of 5-(2,6-dichloro-4-nitro-phenoxy)-2-methoxy-benzenesulfinic acid (1.0 g, 2.64 mmol) in ethanol was added NaOH (116 mg, 2.89 mmol) and cyclopropylmethyl bromide (1.40 mL, 14.5 mmol). The resulting mixture was stirred at 70° C. for 6 h, then at 50° C. for 20 h and concentrated to dryness. The residue was dissolved in 1 N HCl (40 mL) and extracted with EtOAc (4×40 mL). The combined organic extracts were dried and concentrated. The residue was purified by preparative TLC (CH2Cl2: Hex=4:1) to give the title compound of Step C (160 mg) as a solid. MS (APCI−) Calc.: 431.0, Found: 430.2 (M−1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07202275B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-c7e63ce98f184ea591edb0d28b3770cd |
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| Source note | uspto-grants-2007_04 |
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