HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1862246Generated: November 2, 2026
Dichloromethane → 3-Acetoxy-2-(methoxycarbonyl)methoxypyridine
https://huagongshe.com/reaction/1862246
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | Tert-Butyl nitrite | HCID 10906 | — |
| Reactant | 3-Amino-2-(methoxycarbonyl)methoxypyridine | HCID 12115512 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Solvent | Pentane | HCID 8003 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 3-Acetoxy-2-(methoxycarbonyl)methoxypyridine | HCID 12115513 | 36.4% |
Reaction Steps
1.6 g of boron trifluoride diethyl etherate was added to a mixture of 1.0 g of 3-amino-2-(methoxycarbonyl)methoxypyridine, 3 ml of 1,2-dimethoxyethane and 1 ml of dichloromethane dropwise at −10° C. The mixture was stirred for 10 minutes at the same temperature, then, to the reaction solution was added a solution of 0.68 g of t-butyl nitrite in 1 ml of 1,2-dimethoxyethane dropwise at −5° C. or lower. The mixture was stirred for 30 minutes at the same temperature, then, into the mixture was poured n-pentane. The lower layer of two separated layers was dissolved in 5 ml of acetic anhydride, and the mixture was stirred for 1 hour at 80° C. The solvent was distilled off, then, the resulted residue was subjected to silica gel chromatography to obtain 0.45 g of 3-acetoxy-2-(methoxycarbonyl)methoxypyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06537948B1 |
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| Source dataset | uspto-grants-2003_03 |
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| ORD ID | ord-4940deffccc8447e857ef24154566f87 |
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| Source note | uspto-grants-2003_03 |
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