HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1784152Generated: October 30, 2026
Diisopropylethylamine → HCID 22600462, compound
https://huagongshe.com/reaction/1784152
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-(2-Methoxy-ethoxymethyl)-6-trifluoromethyl-nicotinic acid | HCID 11334953 | — |
| Reactant | HCID 57591513 | HCID 57591513 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | HCID 22600462 | HCID 22600462 | — |
Reaction Steps
A mixture of 27 g of a 6.2% solution of 4-bromobicyclo[3.2.1]oct-3-en-2-one (Preparation Example P1) in chlorobenzene, 110 mg of ZnCl2, 2.34 g of 2-methoxyethoxymethyl-6-trifluoromethylnicotinic acid and 1.2 g of Hünig's base is stirred at room temperature under a nitrogen atmosphere until a dark-brown solution is formed. The reaction mixture is then maintained under moderate reflux for 19 hours in an oil bath, with stirring. The mixture is then divided into 2 portions. To one portion there are added a further 1.12 g of 2-methoxyethoxymethyl-6-trifluoromethylnicotinic acid, 0.06 g of ZnCl2 and 0.6 g of Hünig's base. The reaction mixture is then maintained under moderate reflux for 12 hours in an oil bath, with stirring. The solution is then washed twice with 0.1M hydrochloric acid (20 ml each time) and twice with water (20 ml each time). After drying the organic solution using magnesium sulfate and concentrating in vacuo, 3.9 g of 4-(2-methoxyethoxymethyl-6-trifluoromethyl-pyridin-3-ylcarbonyloxy)-bicyclo[3.2.1]oct-3-en-2-one are obtained in the form of a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07501544B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-490092c910054855818fdd351ad58b33 |
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| Source note | uspto-grants-2009_03 |
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