HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1487938Generated: October 31, 2026
Chlorotrimethylsilane → HCID 1534791, compound
https://huagongshe.com/reaction/1487938
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | 4-Bromoaniline | HCID 7807 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,2-Hydrazinedicarboxaldehyde | HCID 12342 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 1534791 | HCID 1534791 | 72% |
Reaction Steps
Into a 100-mL round-bottom flask, was placed a solution of 4-bromoaniline (1.71 g, 9.94 mmol), N′-formylformohydrazide (2.64 g, 30.0 mmol), and triethylamine (9.74 mL, 69.9 mmol, 7.00 equiv) in pyridine (40 mL). Chlorotrimethylsilane (19.2 mL, 151 mmol) was added drop-wise and the resulting solution was stirred for 18 h at 100° C., then cooled to room temperature. The resulting mixture was concentrated under reduced pressure and the residue was diluted with brine (50 mL) and extracted with ethyl acetate (6×50 mL). The combined organic layers were dried (Na2SO4), filtered, and concentrated under reduced pressure. The residue was washed with ether (30 mL) and the solids were collected by filtration to yield the title compound as a pink solid (1.6 g, 72%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09428502B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-a726db9da34e4193a3a4f682be866ada |
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| Source note | uspto-grants-2016_08 |
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