HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 599847Generated: October 30, 2026
Hydrochloric Acid → HCID 59139173, compound
https://huagongshe.com/reaction/599847
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 59139219 | HCID 59139219 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59139173 | HCID 59139173 | 42.6% |
Reaction Steps
THF (0.9 mL) was added to dimethylcarbamic acid 3-(2-fluoro-3-nitrobenzyl)-4-methyl-2-oxo-2H-1-benzopyran-7-yl ester (compound 1g-1-4) (47.6 mg), and the resultant suspension was stirred at −78° C. for 20 minutes to yield a dark brown solution. This solution was added at 0° C. to a solution of N-bromosuccinimide (28 mg) in THF (0.8 mL) (which had been prepared in advance in a separate container), and the mixture was stirred at 0° C. for 40 minutes. This reaction solution was poured into 1N hydrochloric acid (0.119 mL) diluted with ice water (20 mL), and then extracted with ethyl acetate. The organic layer extraction liquid was washed with saturated saline, and the organic layer was dried over anhydrous magnesium sulfate. The solvent was distilled away under reduced pressure, and the resultant residue was purified by thin layer silica gel chromatography (hexane:ethyl acetate=1:1) to yield the title compound (24.3 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07897792B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-74bd7dd656e140128c7dcc60f0c85a51 |
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| Source note | uspto-grants-2011_03 |
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