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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 427248Generated: October 30, 2026

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

https://huagongshe.com/reaction/427248

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantCalcium ChlorideHCID 5284359—
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—
SolventTolueneHCID 1140—
Productmethyl N-[2-chloro-5-(3-chloro-3-methyl-1-butynyl)benzyl]carbamateHCID 15483921133.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

0.50 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 0.15 g of calcium chloride, 0.11 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 reaction 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 residue was purified by silica gel column chromatography to obtain 0.54 g of methyl N-[2-chloro-5-(3-chloro-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-e8a45200b82a4fc09418651423902fc6
Source noteuspto-grants-2001_11