HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355404Generated: October 28, 2026
Butanedioic acid, 2-acetyl-, 1,4-diethyl ester → HCID 86753278, compound
https://huagongshe.com/reaction/355404
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Butanedioic acid, 2-acetyl-, 1,4-diethyl ester | HCID 66197 | — |
| Reactant | 2,4-Difluororesorcinol | HCID 10844515 | — |
| Solvent | Methanesulfonic Acid | HCID 6395 | — |
| Product | HCID 86753278 | HCID 86753278 | 40% |
Reaction Steps
Diethyl acetylsuccinate (2.4 g, 11.1 mmol) is added to a solution of Compound 4 (1.3 g, 8.9 mmol) in 20 mL methanesulfonic acid at 20° C. The reaction is stirred for 16 hours and poured into 200 mL ice water. The product is extracted with EtOAc (80 mL×2), washed with brine (40 mL), dried over anhydrous MgSO4, and concentrated in vacuo to yield a brown oil. The crude oil is purified by column chromatography on silica gel eluted with CHCl3 /MeOH (95:5 to 90:10) to yield 1.06 g (40%) of Compound 10 as an off-white solid. 1H-NMR (DMSO-d6) δ 7.56 (d, 1H), 4.08 (q, 2H), 3.67 (s, 2H), 2.34 (s, 3H), 1.19 (t, 3H). 19F-NMR (DMSO-d6) Φ 130.13 (t, 1F), 148.87 (d, 1F). Also isolated from the column is 0.50 g (20%) of 6,8-difluoro-7-hydroxy-4-methylcoumarin 3-acetic acid (Compound 11).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05830912 |
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| Source dataset | uspto-grants-1998_11 |
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| ORD ID | ord-31efe3a9e7944717b6abdb03f0f724f2 |
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| Source note | uspto-grants-1998_11 |
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