HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412706Generated: October 29, 2026
Dimethylformamide → Ethyl 2-(3-tert-butoxycarbonylpropoxy)benzoate
https://huagongshe.com/reaction/412706
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Ethyl Salicylate | HCID 8365 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Butanoic acid, 4-chloro-, 1,1-dimethylethyl ester | HCID 527695 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ethyl 2-(3-tert-butoxycarbonylpropoxy)benzoate | HCID 18537757 | 62% |
Reaction Steps
A mixture comprising ethyl salicylate (3.14 g, 18.9 mmol) and cesium carbonate (6.2 g, 18.9 mmol), dimethylformamide (25 mL) and tert-butyl 4-chlorobutyrate (4.08 g, 22.8 mmol) was heated at 70° C. and stirred for 12 hours. The mixture was partitioned between ethyl ether (100 mL) and water and the organic layer was separated and washed with additional water (3×) and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo to afford a colorless oil. The residue was purified by silica gel flash chromatography using pure hexane to (10:1) hexane:ethyl acetate to provide ethyl 2-(3-tert-butoxycarbonylpropoxy)benzoate (3.6 g, 62% yield) as a colorless oil; 1H NMR (300 MHz, CDCl3): 7.80 (d, 1H), 7.49 (tr, 1H), 7.00 (m, 2H), 4.40 (q, 2H), 4.10 (tr, 2H), 2.50 (tr, 2H), 2.10 (m, 2H), 1.45 (s, 9H), 1.40 (tr, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06562854B2 |
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| Source dataset | uspto-grants-2003_05 |
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| ORD ID | ord-d8acf5dfa19e4c43a2715c2f0fd46bf3 |
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| Source note | uspto-grants-2003_05 |
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