HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 723556Generated: October 29, 2026
Triethylsilane → 4-(4-Bromomethylbenzyl)-nitrobenzene
https://huagongshe.com/reaction/723556
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | Trifluoromethanesulfonic acid | HCID 62406 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-Bromomethyl-4'-nitrobenzophenone | HCID 14377548 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(4-Bromomethylbenzyl)-nitrobenzene | HCID 21877012 | 56.5% |
Reaction Steps
4-(4-bromomethylbenzoyl)-nitrobenzene (500 mg) was dissolved in dichloromethane (5 mL) and stirred under argon. A solution of trifluoromethanesulfonic acid (0.27 mL) in dichloromethane (2 mL) was added dropwise, followed by a solution of triethylsilane (0.37 mL) in dichloromethane (2 mL). After 5 minutes, a second portion of trifluoromethanesulfonic acid and triethylsilane (same proportions) was added. The reaction mixture was stirred at room temperature for 3 hours, poured into excess aqueous sodium bicarbonate, and extracted with dichloromethane (3×). The solution containing the crude product was evaporated, chromatographed on silica gel, eluting the product with hexane/ethyl acetate, and evaporated to dryness, to give 4-(4-bromomethylbenzyl)-nitrobenzene (270 mg, 56%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07141584B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-1493f0fa4fd9451fb3f5b7f9ccc6bf91 |
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| Source note | uspto-grants-2006_11 |
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