HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1940267Generated: October 26, 2026
Triethylamine → 3-(cyclopentyloxy)-N-(2,6-difluorophenyl)-4-methoxybenzamide
https://huagongshe.com/reaction/1940267
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,6-Difluoroaniline | HCID 79647 | — |
| Reactant | 3-(Cyclopentyloxy)-4-methoxybenzoyl chloride | HCID 2794600 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(cyclopentyloxy)-N-(2,6-difluorophenyl)-4-methoxybenzamide | HCID 9798336 | 46.5% |
Reaction Steps
A stirred solution of 2,6-difluoroaniline (1.52 g) and triethylamine (1.19 g) in dichloromethane (50 mL) at room temperature is treated dropwise with a solution of 3-cyclopentyloxy-4-methoxybenzoyl chloride (3.0 g), that is prepared as described hereinafter in Reference Example 3) in dichloromethane (50 mL). The solution is stirred and heated at reflux for 4 hours, then it is cooled, washed with water and dried over magnesium sulfate. The solution is concentrated and the resulting residue is recrystallized from ethyl acetate, to give N-(2,6-difiuorophenyl)-3-cyclopentyloxy-4-methoxybenzamide (1.9 g), m.p. 158°-160° C. [NMR(CDCl3): 1.55-1.7(m,3H),1.8-2.05(m,5H), 3.93(s,3H),4.85(m,1H),6.9(d,1H),6.95-7.03(m,2H), 7.2-7.3(m,1H),7.3(bs,1H), 7.45(q,1H),7.53(d,1H); Elemental analysis: C,65.1; H,5.6;F, 10.4; N,4.2%; Calculated: C,65.7; H,5.5; F, 10.9; N,4.0%];
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05698711 |
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| Source dataset | uspto-grants-1997_12 |
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| ORD ID | ord-c60e3ab57ac14a32801ced3e7d8b11a0 |
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| Source note | uspto-grants-1997_12 |
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