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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1987906Generated: October 30, 2026

Sodium Iodide → HCID 58980844, compound

https://huagongshe.com/reaction/1987906

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Methoxy-4-nitrophenolHCID 76738—
ReactantN-Boc-2-chloroethylamineHCID 3795708—
ReactantPotassiumHCID 5462222—
SolventDimethylformamideHCID 6228—
ProductHCID 58980844HCID 58980844—

Reaction Steps

A suspension of K2CO3 (280 mg, 2 mmol), NaI (700 mg, 5 mmol), the potassium salt of 2-methoxy-4-nitrophenol (1.37 g, 6.6 mmol), and t-butyl 2-chloroethylcarbamate (1.4 g, 8 mmol) in DMF (8 mL) was heated at 90° C. for 6 hr. After dilution with H2O, the mixture was extracted 4× with CH2Cl2. The combined organic layers were washed 2× with aq. K2CO3, then with brine prior to drying over Na2SO4. After removal of the solvent under vacuum, the residue was chromatographed on silica gel using 5% EtOAc/CH2Cl2 to elute 870 mg of nitrophenyl ether. Pd catalyzed reduction in ethanol as described in step C of Example 6 yielded tert-butyl 2-(4-amino-2-methoxyphenoxy)ethylcarbamate (700 mg) as an off white solid which was carried forward without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07553836B2
Source datasetuspto-grants-2009_06
ORD IDord-d6b5c9ac70cc4553bad653c5a4088120
Source noteuspto-grants-2009_06