HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 729258Generated: October 30, 2026
Diethyl Oxalate → HCID 67243377, compound
https://huagongshe.com/reaction/729258
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Oxalate | HCID 7268 | — |
| Reactant | N-(2-methoxyethyl)-1-phenylmethanesulfonamide | HCID 4467329 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67243377 | HCID 67243377 | 6.1% |
Reaction Steps
A solution of N-(2-methoxyethyl)-1-phenylmethanesulfonamide (3.5 g, 14.5 mmol) and diethyl oxalate (2.33 g, 16.0 mmol) in dry DMF was cooled in an ice-bath. Potassium tert-butoxide (2.17 g, 18.4 mmol) was added and after 5 min the ice-bath was removed and the reaction was stirred at rt for 22 h. HCl (2M, 45 mL) was added to the mixture and the acidic solution was extracted 3 times with DCM. The combined organic layer was washed 4 times with water, dried through a phase separator and evaporated. The residue was purified by preparative HPLC [0.1M N OAc/MeCN, gradient A:B (9:1 to 1:9)] to give the title compound (0.250 g, 6%) as a solid; 1H NMR (500 MHz, CD3OD): δ 7.90-7.94 (m, 2H), 7.28-7.33 (m, 2H), 7.10-7.15 (m, 1H), 3.79 (t, 2H), 3.68 (t, 2H), 3.34 (s, 3H); Mass Spectrum: M−H+ 282.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07582629B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-1b86e9767d8449e5a154d4d65d87c66c |
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| Source note | uspto-grants-2009_09 |
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