HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 610390Generated: October 25, 2026
Dichloromethane → 3-Bromo-6-methoxychroman-4-one
https://huagongshe.com/reaction/610390
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 6-methoxy-3,4-dihydro-2H-1-benzopyran-4-one | HCID 4612168 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 3-Bromo-6-methoxychroman-4-one | HCID 12387307 | 80% |
Reaction Steps
To a solution of 6-methoxy-4-chromanone (35 g) in ethyl ether (1.6 liters) at 5-101 C. was added dropwise over 30 minutes 10.6 ml of bromine. The mixture was stirred at 5-10° C. for 30 minutes and then allowed to warm to room temperature. After 2 hours tlc (CH2Cl2) indicated formation of less polar products and only a trace of starting material remaining. The reaction mixture was washed with water (1 liter), saturated NaHCO3 (500 ml), and brine (500 ml). dried over MgSO4, and concentrated in vacuo to a yellow solid. The crude product was purified by silica gel flash column chromatography on 2.4 Kg fine silica gel, eluting with a gradient system consisting of 3:1 hexanes/dichloromethane followed by 2:1 hexanes/dichloromethane and finally 30% hexanes/dichloromethane. This afforded title product as a yellow solid in 80% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05998451 |
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| Source dataset | uspto-grants-1999_12 |
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| ORD ID | ord-45c2c201f26f4183a90a6b5a0df03e85 |
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| Source note | uspto-grants-1999_12 |
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