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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644289Generated: October 30, 2026

Potassium Iodide → Methyl 2-(3-tert-Butoxycarbonylaminopropoxy)-4-tert-butylbenzoate

https://huagongshe.com/reaction/644289

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactanttert-butyl N-(3-bromopropyl)carbamateHCID 4460490—
ReactantMethyl 4-tert-butyl-2-hydroxybenzoateHCID 20777194—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-(3-tert-Butoxycarbonylaminopropoxy)-4-tert-butylbenzoateHCID 6853019045.2%

Reaction Steps

Methyl 4-tert-butyl-2-hydroxybenzoate (2.41 g, 11.6 mmol) was dissolved in DMF (15 mL) and K2 CO3 (2.39 g, 17.4 mmol) and N-Boc-3-bromopropylamine (4.14 g, 17.4 mmol) was added using DMF (10 mL) to aid the transfer. Potassium iodide (0.30 g) was added, and the reaction stirred at room temperature under nitrogen for 18 hr. The DMF was removed in vacuo and the residue taken up in ethyl acetate and washed with water and brine, dried, and the solvent removed in vacuo to give a viscous brown oil. Purification by chromaotgraphy over silica on a preparative scale apparatus, eluting with a gradient of hexane to hexane:ethyl acetate (70:30) gave 1.91 g (45.2%) of a viscous yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700628B2
Source datasetuspto-grants-2010_04
ORD IDord-77670657196546109d8e761506ef5c33
Source noteuspto-grants-2010_04