HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 658085Generated: October 25, 2026
3-(Bromomethyl)-5-(trifluoromethyl)benzonitrile → 3-(Aminomethyl)-5-(trifluoromethyl)benzonitrile
https://huagongshe.com/reaction/658085
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-(Bromomethyl)-5-(trifluoromethyl)benzonitrile | HCID 11601369 | — |
| Reactant | Ammonia methanol | HCID 21705897 | — |
| Product | 3-(Aminomethyl)-5-(trifluoromethyl)benzonitrile | HCID 45115840 | — |
Reaction Steps
3-Bromomethyl-5-trifluoromethyl-benzonitrile (which is prepared in Reference Example 12) (15.9 g) is dissolved in 7M-ammonia/methanol (550 ml), and the mixture is stirred at 50-60° C. for 30 minutes. The reaction solution is concentrated under reduced pressure. To the resulting residue are added a saturated aqueous sodium bicarbonate solution and chloroform, and the mixture is separated, and the organic layer is dried over sodium sulfate, and concentrated under reduced pressure. The resulting residue is purified by silica gel column chromatography (chloroform:methanol=1:0→19:1→chloroform:methanol:ammonium hydroxide solution=19:1:0.1) to give 3-aminomethyl-5-trifluorometyl-benzonitrile (10.4 g). MS (m/z): 201 [M+H]+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08076364B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-59a4312b22d24405804e93c91807a522 |
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| Source note | uspto-grants-2011_12 |
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