HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 875257Generated: October 31, 2026
Bromochloromethane → HCID 86657995, compound
https://huagongshe.com/reaction/875257
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromochloromethane | HCID 6333 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | HCID 67393369 | HCID 67393369 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86657995 | HCID 86657995 | 101% |
Reaction Steps
2.5 g of bromochloromethane (18.8 mmol) were added at room temperature to a solution of 2.0 g of (R)-6-Fluoro-1-benzopyran-2-carboxylic acid methyl ester, obtained after separation of the corresponding racemic mixture on a chiral chromatography column (9.4 mmol, 96.6% A, ee>99%), in 40 ml THF. The solution was then cooled to −80/−85° C. and 7.7 ml of 2.5 M n-BuLi in hexane (19 mmol) were slowly added to maintain the internal temperature between −75° C. and −80° C. The reaction progress was monitored by TLC. The solution was then acidified by the addition of 2 ml glacial acetic acid in 2 ml THF between −70° C. and −80° C. 10 ml of water were then added at −20/0° C. and the aqueous layer was then removed after decantation. The organic layer was concentrated under reduced pressure to give the title compound (2.2 g) as a white-off solid (ee: 97.2%, 94.8% A).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08981127B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-a5ecc5c4d38d4c52aeef917ae0b16159 |
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| Source note | uspto-grants-2015_03 |
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