HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047982Generated: October 31, 2026
Chlorotrimethylsilane → HCID 58244424, compound
https://huagongshe.com/reaction/1047982
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | (E)-2-methoxy-1-(2-nitrovinyl)-4-(trifluoromethyl)benzene | HCID 67080220 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58244424 | HCID 58244424 | 95.4% |
Reaction Steps
A portion of lithium borohydride (0.458 g, 21.0 mmol) was diluted with THF (30 mL) followed by the dropwise addition of chlorotrimethylsilane (5.34 ml, 42.1 mmol). After stirring for 15 minutes, argon was bubbled through the reaction mixture for 2 minutes to eliminate trimethylsilane present in the reaction. (E)-2-methoxy-1-(2-nitrovinyl)-4-(trifluoromethyl)benzene (1.3 g, 5.26 mmol) was added portionwise (gas evolution occurred). The reaction was heated to reflux for 2 hours, cooled to 0° C. and carefully quenched with methanol (8 mL). The reaction mixture was concentrated, diluted with dichloromethane and 20% aqueous KOH. The layers were separated and the organic layer was dried over sodium sulfate, filtered and concentrated to yield 2-(2-methoxy-4-(trifluoromethyl)phenyl)ethanamine (1.1 g, 5.02 mmol, 95.4% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08569522B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-7e91a51e755f406ea1fb9b6bb4684f59 |
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| Source note | uspto-grants-2013_10 |
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