HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354115Generated: November 1, 2026
Trifluoroacetic acid → HCID 68502963, compound
https://huagongshe.com/reaction/2354115
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Phenol, 2-[(1E)-2-(2-bromophenyl)ethenyl]-4-chloro-, 1-acetate | HCID 44139027 | — |
| Reactant | HCID 86617526 | HCID 86617526 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 68502963 | HCID 68502963 | 96% |
Reaction Steps
trans-2-Bromo-2′-acetoxy-5′-chlorostilbene (26 g, 73 mmol) was slurried in toluene (91 ml) at 33° C. Trifluoroacetic acid (200 microliters) was added. The N-methoxymethyl-N-trimethylsilyl-N-methylamine (14.5 g; 89.7 mmol) was added to the reaction mixture over 90 minutes. After addition, the reaction was washed with water (25 ml). The toluene was removed by vacuum distillation. Ethanol (30 ml) was added and removed under reduced pressure. The oil was dissolved in methanol (90 ml). Potassium hydroxide (5 grams in 25 ml water)) was added. The product began to precipitate immediately. After 30 minutes, the pH was adjusted to 8-9 with 3N HCl (8 ml). Added water (10 ml) and cooled to less than 10° C. Filtered and washed with 1:1 methanol: water. Dried in vacuum to 26.0 grams (96% yield). Purity according to HPLC is 98% a/a.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07750167B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-2b01e92ede874a0d857169e93da74062 |
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| Source note | uspto-grants-2010_07 |
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