HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 427247Generated: November 1, 2026
Sodium Chloride → methyl N-[2-chloro-5-(3-hydroxy-3-methyl-1-butynyl)benzyl]carbamate
https://huagongshe.com/reaction/427247
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | 2-Methyl-3-butyn-2-ol | HCID 8258 | — |
| Reactant | methyl N-[(5-bromo-2-chlorophenyl)methyl]carbamate | HCID 15483918 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | methyl N-[2-chloro-5-(3-hydroxy-3-methyl-1-butynyl)benzyl]carbamate | HCID 15483920 | 85.6% |
Reaction Steps
A mixture comprising 3.50 g of methyl N-(5-bromo-2-chlorobenzyl)carbamate, 2.11 g of 2-methyl-3-butyn-2-ol, 0.79 g of dichlorobis(triphenylphosphine)palladium, 0.38 g of copper(I) iodide and 40 ml of triethylamine, was stirred at 90° C. for 30 hours in an autoclave. This reaction solution was poured into a saturated sodium chloride aqueous solution 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 3.03 g of methyl N-[2-chloro-5-(3-hydroxy-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-b5930c8359604aff81ded6cf72569441 |
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| Source note | uspto-grants-2001_11 |
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