HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17298Generated: October 25, 2026
Dichloromethane → 4-Amino-3-cyano-6-fluoro-5-hydroxy-2-methylbiphenyl
https://huagongshe.com/reaction/17298
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 4-Amino-3-cyano-6-fluoro-5-methoxy-2-methylbiphenyl | HCID 86097441 | — |
| Reactant | HCID 178419199 | HCID 178419199 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Amino-3-cyano-6-fluoro-5-hydroxy-2-methylbiphenyl | HCID 86097446 | 93% |
Reaction Steps
Under nitrogen atmosphere, at −78° C., 1 M borane trifluoride/methylene chloride solution (3.0 ml, 3.0 mmol) was dropwise added to a methylene chloride (10 ml) solution of 4-amino-3-cyano-6-fluoro-5-methoxy-2-methylbiphenyl (I-39) (250 mg, 1.0 mmol), taking 10 minutes, followed by stirring for 4 hours and a half with gradually heating up to 0° C. Water with ice was added to the reaction liquid, followed by neutralization at pH of 7 with aqueous 10% sodium carbonate solution and extraction three times with chloroform, the organic layer was washed with saturated brine, then dried over anhydrous magnesium sulfate. After filtration and concentration under reduced pressure, the resulting residue gave the entitled compound (225 mg, 93%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07737166B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-65bd50426a9e487eb79916c044d4e82c |
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| Source note | uspto-grants-2010_06 |
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