HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1952613Generated: November 2, 2026
Methanol → 5-Diethoxymethyl-3-isopropyl-thiophene-2-carboxylic acid methyl ester
https://huagongshe.com/reaction/1952613
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Methyl Thioglycolate | HCID 16907 | — |
| Reactant | 6,6-Diethoxy-2-methylhex-4-yn-3-one | HCID 341439 | — |
| Reactant | Cs2CO3 MgSO4 | HCID 86671257 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Diethoxymethyl-3-isopropyl-thiophene-2-carboxylic acid methyl ester | HCID 68226612 | 30.4% |
Reaction Steps
A solution of 6,6-Diethoxy-2-methyl-hex-4-yn-3-one (1.32 g, 6.66 mmol) in THF (20 ml) was cooled to 0° C. (ice bath). Methyl thioglycolate (0.6 ml, 6.66 mmol) was added in one portion and the mixture was stirred at 0° C. for 1 h. Methanol (3 ml) and Cs2CO3/MgSO4 (1 g/2 g, pre-dried at 200° C. in vacuum) were added at 0° C. The mixture was stirred at 0° C. for 15 min and then at rt for 15 h. The reaction mixture was quenched by pouring into EtOAc. The organic layer was washed with brine, dried over Na2SO4 and concentrated under reduced pressure. The residue was purified by flash chromatography with 0-20% EtOAc in hexane to afford the desired product (0.58 g, 30% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08404859B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-88701c756fb3448292c6b019790e70f4 |
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| Source note | uspto-grants-2013_03 |
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