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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1062475Generated: October 25, 2026

Hydrochloric Acid → 5-(2,6-Dichloro-4-methoxymethyl-phenoxy)-2-methoxy-benzoic acid

https://huagongshe.com/reaction/1062475

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-Methyl-2-buteneHCID 10553—
Reactant5-(2,6-Dichloro-4-methoxymethyl-phenoxy)-2-methoxy-benzaldehydeHCID 22285657—
ReactantSodium HypochloriteHCID 23665760—
SolventMonobasic potassium phosphateHCID 516951—
SolventTert-butanol tetrahydrofuranHCID 66775918—
Product5-(2,6-Dichloro-4-methoxymethyl-phenoxy)-2-methoxy-benzoic acidHCID 22285652100.7%

Reaction Steps

To a solution of the title compound of Step C (228 mg, 0.67 mmol) and 2-methyl-2-butene (2M in tetrahydrofuran, 5 ml, 10.0 mmol) in tert-butanol/tetrahydrofuran (1 ml/3 ml) was added slowly a solution of sodium hypochlorite (543 mg, 6.0 mmol) in potassium dihydrogen phosphate aqueous solution (0.6 M, 8 ml). The reaction mixture was stirred for one hour at room temperature. The mixture was acidified with 1N HCl and extracted with ethyl acetate (3×20 ml). The combined organic extracts were washed with 1N HCl (2×40 ml), brine (40 mL), dried, filtered, and concentrated to afford the title compound (241 mg) as a viscous oil which was used in the next step without further purification. MS (APCI−) Calc: 356.0, found: 355.0 (M−1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06960604B2
Source datasetuspto-grants-2005_11
ORD IDord-a8497c5ee3c742dfb136a080c96a7456
Source noteuspto-grants-2005_11