HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 394439Generated: October 28, 2026
Potassium Carbonate → Allyl 2-[2-chloro-5-(3,5-dimethyl-2,6-dioxo-[1,3,5]triazinan-1-yl)-4-fluorophenoxy]propionate
https://huagongshe.com/reaction/394439
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Prop-2-en-1-yl 2-bromopropanoate | HCID 12882383 | — |
| Reactant | 3-(4-Chloro-2-fluoro-5-hydroxyphenyl)-1,5-dimethyl-6-thioxo-[1,3,5]triazinane-2,4-dione | HCID 18176016 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Allyl 2-[2-chloro-5-(3,5-dimethyl-2,6-dioxo-[1,3,5]triazinan-1-yl)-4-fluorophenoxy]propionate | HCID 18176013 | — |
Reaction Steps
0.37 g (2.65 mmol) of K2CO3 and 0.51 g (2.65 mmol) of rac. allyl 2-bromopropionate were added approximately at 20° C. to a solution of 0.80 g (2.52 mmol) of 3-(4-chloro-2-fluoro-5-hydroxyphenyl)-1,5-dimethyl-6-thioxo-[1,3,5]triazinane-2,4-dione in 15 ml of dimethylformamide. After the reaction mixture had been stirred for two hours at approximately 20° C., it was stirred into ice-water. The product was extracted three times with methyl tert-butyl ether. The combined organic phases were dried over magnesium sulfate and then concentrated. The crude product (1.18 g) was purified by column chromatography (mobile phase: cyclohexane/ethyl acetate=15:1). Yield: 0.88 g (81%); 1H NMR (270 MHz, in CDCl3): δ[ppm]=1.7 (d, 3H), 3.8 (s, 6H), 4.6 (m, 2H), 4.7 (q, 1H), 5.2 (d, 1H), 5.3 (d, 1H), 5.9 (m, 1H), 6.9 (d, 1H), 7.3 (d, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06602825B1 |
|---|
| Source dataset | uspto-grants-2003_08 |
|---|
| ORD ID | ord-47e3ae328624462499b721e8cc85f8f7 |
|---|
| Source note | uspto-grants-2003_08 |
|---|