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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Calcium Chloride | HCID 5284359 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | methyl N-[2-chloro-5-(3-hydroxy-3-methyl-1-butynyl)benzyl]carbamate | HCID 15483920 | — |
| Catalyst | Copper | HCID 23978 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | methyl N-[2-chloro-5-(3-methoxy-3-methyl-1-butynyl)benzyl]carbamate | HCID 15483922 | 82.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06313071B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-295b57c1a31a45b8be65cd46c174eb80 |
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| Source note | uspto-grants-2001_11 |
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