HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1648104Generated: November 1, 2026
Potassium Carbonate → [(2,3-Dihydro-3-oxo-1H-naphtho[2,1-b]pyran-8-yl)oxy]acetic Acid 1,1-Dimethylethyl Ester
https://huagongshe.com/reaction/1648104
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | tert-Butyl bromoacetate | HCID 79177 | — |
| Reactant | 1,2-Dihydro-8-hydroxy-3H-naphtho[2,1-b]pyran-3-one | HCID 19921957 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | [(2,3-Dihydro-3-oxo-1H-naphtho[2,1-b]pyran-8-yl)oxy]acetic Acid 1,1-Dimethylethyl Ester | HCID 54520651 | 91% |
Reaction Steps
A mixture of 2.18 g (10.2 mmol) of 1,2-dihydro-8-hydroxy-3H-naphtho[2,1-b]pyran-3-one from the preceding example, 4.84 g (24.8 mmol) of t-butyl bromoacetate, 5.63 g (40.7 mmol) of anhydrous granular potassium carbonate and 55.5 mL of 2-butanone was heated at 60° C. for 24 hr. A second portion of t-butyl bromoacetate (0.5 mL, 3.1 mmol) was added and the reaction was allowed to proceed for another 17 hr. After being cooled to room temperature, the mixture was filtered and the solids were washed with ethyl acetate and ether. The filtrate and washes were combined and concentrated in vacuo, and the crude product was flash chromatographed on 360 g of silica gel, eluting with hexane-ethyl acetate (7:1 then 6:1) affording 3.04 g (91.0%) of the title compound as a white solid, mp 95°-96° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05434186 |
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| Source dataset | uspto-grants-1995_07 |
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| ORD ID | ord-d966d50141bb4db688e42da38fa61368 |
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| Source note | uspto-grants-1995_07 |
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