HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1678298Generated: October 29, 2026
Sodium Iodide → [4-(4-Benzyloxycarbonylaminobutyl)phenoxy]acetic acid ethyl ester
https://huagongshe.com/reaction/1678298
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-Cbz4-(4-hydroxyphenyl)butylamine | HCID 11637991 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | [4-(4-Benzyloxycarbonylaminobutyl)phenoxy]acetic acid ethyl ester | HCID 21031128 | 89.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08008494B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-4c83dc19d30c4ceba92d79497d1c92cd |
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| Source note | uspto-grants-2011_08 |
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