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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1175717Generated: November 2, 2026

Sodium Iodide → [4-(4-Benzyloxycarbonylaminobutyl)phenoxy]acetic acid ethyl ester

https://huagongshe.com/reaction/1175717

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
ReactantN-Cbz4-(4-hydroxyphenyl)butylamineHCID 11637991—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product[4-(4-Benzyloxycarbonylaminobutyl)phenoxy]acetic acid ethyl esterHCID 2103112889.1%

Reaction Steps

A solution of [4-(4-hydroxyphenyl)butyl]carbamic acid benzyl ester (2.0 g, 6.7 mmol), potassium carbonate (1.0 g, 7.3 mmol), sodium iodide (0.4 g, 2.7 mmol), and DMF (10 mL) was stirred for 30 minutes. A solution of ethyl bromoacetate (0.8 mL, 7.4 mmol) in DMF (10 mL) was added dropwise to the reaction. The reaction was further stirred at room temperature for 3 days, and then poured into water (200 mL). The product was extracted with ethyl acetate. The organic layer was dried over sodium sulfate and concentrated in vacuo. The residue was purified by flash chromatography (silica gel, 1:5 ethyl acetate/hexanes, v/v) to provide the desired product 33 (2.3 g, 89%) as a white solid. 1H NMR (300 MHz, CDCl3) δ 1.34 (t, 3H), 1.57 (m, 4H), 2.56 (t, 2H), 3.20 (q, 2H), 4.25 (q, 2H), 4.59 (s, 2H), 5.10 (s, 2H), 6.85 (d, 2H), 7.06 (d, 2H), 7.38 (m, 5H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842697B2
Source datasetuspto-grants-2010_11
ORD IDord-c2a70f09679f4bf2aac486137af261fb
Source noteuspto-grants-2010_11