HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743974Generated: October 30, 2026
Bromochloromethane → HCID 22236954, compound
https://huagongshe.com/reaction/1743974
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromochloromethane | HCID 6333 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | HCID 22236944 | HCID 22236944 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22236954 | HCID 22236954 | 80% |
Reaction Steps
A solution of 20 g of the compound obtained in Step 1 in 400 ml of THF was stirred at −78° C. under atmosphere of nitrogen, and then, 45 ml of 2M lithium diisopropylamide solution was slowly added thereto. The resulting mixture was stirred for one hour and thereto was slowly added a solution of 13.62 g of bromochloromethane in 30 ml of THF. After one hour, the resulting mixture was stirred at room temperature for four hours. After the reaction was completed, an aqueous ammonium chloride solution was added, the reaction mixture was extracted with ethyl acetate. The organic phase was dried over anhydrous magnesium sulfate and concentrated under reduced pressure, and the residue thus obtained was purified by a silica gel column chromatography using a mixture of ethyl acetate and n-hexane of 1:6 to obtain 19.14 g of the title compound as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07012144B2 |
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| Source dataset | uspto-grants-2006_03 |
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| ORD ID | ord-a46adac91750492daf48648a0f582394 |
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| Source note | uspto-grants-2006_03 |
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