HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2120307Generated: October 30, 2026
Diethyl Oxalate → N-{4-[3-(4-fluorobenzenesulfonyl)-4-hydroxyphenoxy]-3,5-dimethylphenyl}oxamic acid ethyl ester
https://huagongshe.com/reaction/2120307
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Oxalate | HCID 7268 | — |
| Reactant | 4-(4-Amino-2,6-dimethylphenoxy)-2-(4-fluorobenzenesulfonyl)phenol | HCID 22344876 | — |
| Product | N-{4-[3-(4-fluorobenzenesulfonyl)-4-hydroxyphenoxy]-3,5-dimethylphenyl}oxamic acid ethyl ester | HCID 10163263 | — |
Reaction Steps
A mixture of the title D compound, 4-(4-amino-2,6-dimethylphenoxy)-2-(4-fluoro-benzenesulfonyl)phenol (0.64 g, 1.65 mmol) and 2 mL of diethyl oxalate is heated at 180° C. for 3 h. The reaction is cooled to RT and diethyl oxalate is removed under vacuum. Chromatography on silica (eluant; EtOAc/hexane—1/3?2/3) affords N-{4-[3-(4-fluoro-benzenesulfonyl)-4-hydroxyphenoxy]-3,5-dimethylphenyl}oxamic acid ethyl ester: NMR (CDCl3) 1.46 (t, 3H, J=7.5), 2.06 (s, 6H), 4.42 (q, 2H, J=7.5), 6.90-6.98 (m, 3H), 7.22 (app t, 2H, J=8.3), 7.40 (s,2H), 7.87-7.93 (m, 2H), 8.87 (br s, 1H); ESI-MS 486 [M−1]−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06689896B2 |
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| Source dataset | uspto-grants-2004_02 |
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| ORD ID | ord-320bf583ee33483281dd782af6c5a3e9 |
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| Source note | uspto-grants-2004_02 |
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