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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644271Generated: October 28, 2026

Potassium Iodide → Methyl 2-(3-tert-butoxycarbonylaminopropoxy)-4-methoxybenzoate

https://huagongshe.com/reaction/644271

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantMethyl 4-methoxysalicylateHCID 79523—
Reactanttert-butyl N-(3-bromopropyl)carbamateHCID 4460490—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-(3-tert-butoxycarbonylaminopropoxy)-4-methoxybenzoateHCID 6853405993.3%

Reaction Steps

To a solution of methyl 4-methoxysalicylate (11.48 g, 63 mmol) in dimethylformamide (30 mL) was added solid K2 CO3 (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 HPLC chromatograph 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700628B2
Source datasetuspto-grants-2010_04
ORD IDord-d1c520cada8b4d359ab555a6c09abf7d
Source noteuspto-grants-2010_04