HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1438086Generated: November 1, 2026
1-(Bromomethyl)-2-(trifluoromethyl)benzene → HCID 57941473, compound
https://huagongshe.com/reaction/1438086
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-(Bromomethyl)-2-(trifluoromethyl)benzene | HCID 123057 | — |
| Reactant | HCID 57941345 | HCID 57941345 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 57941473 | HCID 57941473 | 56.4% |
Reaction Steps
A solution of (4R,7S)-1-benzyl-7,8,8-trimethyl-1,2,4,5,6,7-hexahydro-4,7-methano-indazol-3-one (Intermediate 49; 96 mg, 0.33 mmol) and 2-(trifluoromethyl)benzyl bromide (85 mg, 0.35 mmol) in dimethylformamide (3.4 mL) was heated at 100° C. for 24 h. A second portion of 2-(trifluoromethyl)benzyl bromide (85 mg, 0.35 mmol) was added and the mixture was heated at 110° C. overnight. The solvent was evaporated and dichloromethane (100 mL) was added. The solution was washed with saturated aqueous sodium thiosulfate (150 mL), saturated aqueous sodium hydrogen carbonate (150 mL) and brine (150 mL), dried (sodium sulfate), filtered, evaporated and purified using a Biotage 40S system, eluting with 2% methanol/dichloromethane, to give (4R,7S)-1-benzyl-7,8,8-trimethyl-2-(2-trifluoromethyl-benzyl)-1,2,4,5,6,7-hexahydro-4,7-methano-indazol-3-one (82 mg, 55%) as an off-white solid. APCI(+)-MS (M+H) 441.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07622492B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-c61930a5798646a5be7b9b8e4b10e788 |
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| Source note | uspto-grants-2009_11 |
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