HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 540652Generated: October 28, 2026
2-Bromo-naphtho[2,3-b]furan-4,9-dione → 2-Methylthio-naphtho[2,3-b]furan-4,9-dione
https://huagongshe.com/reaction/540652
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromo-naphtho[2,3-b]furan-4,9-dione | HCID 396287 | — |
| Reactant | Mesna | HCID 23662354 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Methylthio-naphtho[2,3-b]furan-4,9-dione | HCID 10776673 | 90.1% |
Reaction Steps
To the solution of 0.7 gram (2.5 mmoles) of 2-bromo-naphtho[2,3-b]furan-4,9-dione in 20 mL of tetrahydrofuran at room temperature, 0.4 grams (5.0 mmoles) of MeSNa in 5 mL of water was added dropwise over 1 minute. The mixture was further stirred for 2 hours at room temperature, and then evaporated to remove tetrahydrofuran. To the residue, 20 mL of 1N hydrochloric acid was added, and the resulting mixture was filtered. The solid was washed with water, and then crystallized in ethanol/water. Pure crystal product was filtered and dried under vacuum. 0.55 grams of product (yield 90%) was obtained and characterized by 1H NMR and mass spectrum. 1H NMR (in CDCl3) δ 2.66 (s, 3H), 6.79 (s, 1H), 7.75-7.79 (m, 2H), 8.18-8.25 (m, 2H). Mass (M+H) is 245.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08871802B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-ced5cc5c55bd4c3b8a67026cd95b98e1 |
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| Source note | uspto-grants-2014_10 |
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