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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 427249Generated: October 30, 2026

Hydrochloric Acid → methyl N-[2-chloro-5-(3-methoxy-3-methyl-1-butynyl)benzyl]carbamate

https://huagongshe.com/reaction/427249

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantCalcium ChlorideHCID 5284359—
ReactantSodium MethoxideHCID 10942334—
Reactantmethyl N-[2-chloro-5-(3-hydroxy-3-methyl-1-butynyl)benzyl]carbamateHCID 15483920—
CatalystCopperHCID 23978—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Productmethyl N-[2-chloro-5-(3-methoxy-3-methyl-1-butynyl)benzyl]carbamateHCID 1548392282.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

0.60 g of methyl N-[2-chloro-5-(3-hydroxy-3-methyl-1-butynyl)benzyl]carbamate was dissolved in 10 ml of toluene. This solution was added at 0° C. to a mixture comprising 0.12 g of calcium chloride, 0.08 g of copper(I) iodide, 0.01 g of copper and 10 ml of concentrated hydrochloric acid, followed by stirring at 0° C. for 5 hours. This solution was poured into water and extracted with ethyl acetate, followed by drying over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the obtained crude product was dissolved in 10 ml, of methanol. To this solution, 0.50 g of sodium methylate (28 wt % methanol solution) was added at room temperature, followed by stirring at room temperature for 24 hours. The reaction mixture was poured into water and extracted with ethyl acetate, followed by drying over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified with silica gel column chromatography to obtain 0.52 g of methyl N-[2-chloro-5-(3-methoxy-3-methyl-1-butynyl)benzyl]carbamate as a brown viscous liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313071B1
Source datasetuspto-grants-2001_11
ORD IDord-295b57c1a31a45b8be65cd46c174eb80
Source noteuspto-grants-2001_11