HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1970293Generated: November 2, 2026
Diethyl Ether → 8-Bromo-2-chloro-10-methylene-10h-chromeno[3,2-b]pyridine
https://huagongshe.com/reaction/1970293
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | 8-bromo-2-chloro-10H-chromeno[3,2-b]pyridin-10-one | HCID 58466196 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 8-Bromo-2-chloro-10-methylene-10h-chromeno[3,2-b]pyridine | HCID 58466187 | — |
Reaction Steps
To a suspension of 8-bromo-2-chloro-10H-chromeno[3,2-b]pyridin-10-one (20 g, 64.4 mmol) in 500 mL of THF at −78° C. was added dropwise methylmagnesium bromide 3.0 M in diethyl ether (13.82 mL, 116 mmol). The reaction was allowed to slowly warmed up to 0° C. in about 2 h. The reaction was quenched with NH4Cl solution, extracted with EtOAc, dried over Na2SO4, filtered and evaporated to give the corresponding crude tertiary alcohol. This solid residue was re-dissolved in 100 mL of THF and treated with mL of chloroform and the resulting solution was evaporated on a 75° C. water bath for 10 min to give crude 8-bromo-2-chloro-10-methylene-10H-chromeno[3,2-b]pyridine as a brownish solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08426447B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-3cc63789030449418d413814e7c59c20 |
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| Source note | uspto-grants-2013_04 |
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