HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 14136Generated: October 26, 2026
Triethylamine → Methyl 3-methyl-5-{[methyl(pentyl)amino]methyl}benzoate
https://huagongshe.com/reaction/14136
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | N-Methylpentylamine | HCID 117479 | — |
| Reactant | Methyl 3-(hydroxymethyl)-5-methylbenzoate | HCID 21086184 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 3-methyl-5-{[methyl(pentyl)amino]methyl}benzoate | HCID 21086189 | — |
Reaction Steps
To an ice-cold, stirred solution of methyl 3-(hydroxymethyl)-5-methylbenzoate (200 mg, 1.1 mmol) in methylene chloride (2.2 mL) is added triethylamine (0.304 mL, 2.2 mmol) followed by methanesulfonyl chloride (0.116 mL, 1.5 mmol). The reaction mixture is stirred for 15 min and filtered. N-Methylpentylamine (333 mg, 3.3 mmol) is added to the filtrate, and the reaction mixture is stirred at room temperature for 5 h. The reaction mixture is diluted with methylene chloride (10 mL), washed with 1 N hydrochloric acid, and saturated sodium bicarbonate, dried (magnesium sulfate), filtered, and concentrated under reduced pressure. Purification by flash column chromatography (silica, 15% ethyl acetate/hexanes) provides the title compound. 1H NMR (300 MHz, CDCl3) δ 7.75 (d, J=4 Hz, 2H), 7.36 (s, 1H), 3.90 (s, 3H), 3.47 (s, 2H), 3.13 (t, J=9 Hz, 3H), 2.39 (s, 2H), 2.34 (d, J=8 Hz, 2H), 2.18 (s, 3H), 1.45 (m, 5H), 1.32 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07727997B2 |
|---|
| Source dataset | uspto-grants-2010_06 |
|---|
| ORD ID | ord-3d2ea35b943343e0ad8cefcd218ac4a0 |
|---|
| Source note | uspto-grants-2010_06 |
|---|