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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354115Generated: November 1, 2026

Trifluoroacetic acid → HCID 68502963, compound

https://huagongshe.com/reaction/2354115

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantPhenol, 2-[(1E)-2-(2-bromophenyl)ethenyl]-4-chloro-, 1-acetateHCID 44139027—
ReactantHCID 86617526HCID 86617526—
SolventTolueneHCID 1140—
ProductHCID 68502963HCID 6850296396%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07750167B2
Source datasetuspto-grants-2010_07
ORD IDord-2b01e92ede874a0d857169e93da74062
Source noteuspto-grants-2010_07