HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 416124Generated: October 29, 2026
Water → tert-Butyl 7-ethoxynaphthalen-1-ylcarbamate
https://huagongshe.com/reaction/416124
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | tert-Butyl (7-hydroxynaphthalen-1-yl)carbamate | HCID 18536180 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | tert-Butyl 7-ethoxynaphthalen-1-ylcarbamate | HCID 59731041 | 67.5% |
Reaction Steps
Next, to a mixture of tert-butyl (7-hydroxy-1-naphthyl)carbamate (64.0 g, 247 mmol) and cesium carbonate (161 g, 493 mmol) in 300 mL anhydrous DMF was added iodoethane (42.3 g, 272 mmol) at room temperature. The mixture was stirred at 60° C. for 2 hours. Water was added to the mixture, and the product was extracted with ethylacetate. The organic layer was washed with water and brine, dried over Na2SO4, filtered, and concentrated under reduced pressure. To the obtained residue was added diisopropyl ether and the precipitate was collected and dried to afford tert-butyl (7-ethoxy-1-naphthyl)carbamate (47.9 g, 67.5% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08088826B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-e1ce4d9ce19b46f2b5d1590c946e4e41 |
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| Source note | uspto-grants-2012_01 |
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