HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1445441Generated: October 30, 2026
Potassium Iodide → Methyl 2-(3-tert-butoxycarbonylaminopropoxy)-4-methoxybenzoate
https://huagongshe.com/reaction/1445441
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 4-methoxysalicylate | HCID 79523 | — |
| Reactant | tert-butyl N-(3-bromopropyl)carbamate | HCID 4460490 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 2-(3-tert-butoxycarbonylaminopropoxy)-4-methoxybenzoate | HCID 68534059 | 93.3% |
Reaction Steps
To a solution of methyl 4-methoxysalicylate (11.48 g, 63 mmol) in dimethylformamide (30 mL) was added solid K2CO3 (13.06 g, 94.5 mmol), 1-tert-butoxycarbonylamino-3-bromopropane (22.5 g, 94.5 mmol), and freshly ground potassium iodide (1.5 g). The resulting slurry was placed under a nitrogen atmosphere and stirred for 2.5 days. The slurry was diluted with water (250 mL), washed with 1 N NaOH (2×250 mL), water (250 mL), and brine (250 mL), then dried over sodium sulfate and concentrated in vacuo. The crude mixture was purified on a preparative (Waters Prep LC™) 500 A chromatography apparatus using two silica columns and a hexanes through 1:1 hexanes:EtOAc gradient to provide methyl 2-(3-tert-butoxycarbonylaminopropoxy)-4-methoxybenzoate (19.93 g, 93.3%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07666866B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-9d997aa51fdc4ad79a5ac6f4e67c6447 |
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| Source note | uspto-grants-2010_02 |
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