HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649939Generated: October 29, 2026
Potassium Iodide → Methyl 5-benzoylamino-5,6,7,8-tetrahydro-naphth-1-yl-oxyacetate
https://huagongshe.com/reaction/1649939
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Methyl chloroacetate | HCID 7295 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-Benzoylamino-1-hydroxy-5,6,7,8-tetrahydro-naphthalene | HCID 14014955 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 5-benzoylamino-5,6,7,8-tetrahydro-naphth-1-yl-oxyacetate | HCID 14014967 | — |
Reaction Steps
50 mmol of 5-benzoylamino-1-hydroxy-5,6,7,8-tetrahydro-naphthalene and 100 ml of anhydrous potassium potassium carbonate are stirred at 50° C. in 100 ml of absolute dimethylformamide for 20 minutes. A solution of 60 mmol of methyl chloroacetate and 25 mmol of potassium iodide in 25 ml dimethylformamide is added dropwise and the mixture is stirred at 50° C. for 6 to 8 hours. It is filtered under the influence of heat, the residue is rinsed thoroughly with ethyl acetate and the filtrate is evaporated. The residue is stirred in a mixture of 10% strength NaOH and ethyl acetate or tetrahydrofuran for 10 minutes. The ethyl acetate phase is extracted by shaking once with 10% strength NaOH, dried over Na2SO4 and evaporated. The residue is recrystallized from ethyl acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04921998 |
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| Source dataset | uspto-grants-1990_05 |
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| ORD ID | ord-f84af81b285a41fa8277dda8c220d603 |
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| Source note | uspto-grants-1990_05 |
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