HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 477598Generated: October 25, 2026
Water → 3-ethoxycarbonylmethyl-6-fluoro-5-nitro-2(3H)-benzothiazolone
https://huagongshe.com/reaction/477598
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 6-fluoro-5-nitro-2(3H)-benzothiazolone | HCID 13957955 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-ethoxycarbonylmethyl-6-fluoro-5-nitro-2(3H)-benzothiazolone | HCID 14014244 | 25% |
Reaction Steps
50% Oily sodium hydride (0.21 g) was suspended in N,N-dimethylformamide (5 ml), and the resultant suspension was cooled to 0° C. 6-Fluoro-5-nitro-2(3H)-benzothiazolone (1.0 g) was portionwise added thereto at 0° C., and the mixture was stirred at the same temperature for 30 minutes. Ethyl bromoacetate (0.86 g) was added to the reaction mixture at 0° C., and the temperature was gradually elevated to a temperature of 50° to 60° C., followed by stirring at that temperature for 3 hours. Water was added to the mixture, which was extracted with ethyl acetate. The extract was washed with water, dried and concentrated. The residue was purified by silica gel thin layer chromatography with a mixture of ethyl acetate and toluene (1:9) to give 0.35 g of 3-ethoxycarbonylmethyl-6-fluoro-5-nitro-2(3H)-benzothiazolone, m.p., 139.0°-140.0° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04888428 |
|---|
| Source dataset | uspto-grants-1989_12 |
|---|
| ORD ID | ord-33779e788a05417badbe4024f628ef3d |
|---|
| Source note | uspto-grants-1989_12 |
|---|