HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1624222Generated: November 3, 2026
Ethyl 4-(mercaptomethyl)-2-methyl-1,3-oxazole-5-carboxylate → 4-(Mercaptomethyl)-2-methyl-1,3-oxazole-5-carbaldehyde
https://huagongshe.com/reaction/1624222
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 4-(mercaptomethyl)-2-methyl-1,3-oxazole-5-carboxylate | HCID 86675540 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(Mercaptomethyl)-2-methyl-1,3-oxazole-5-carbaldehyde | HCID 86675541 | — |
Reaction Steps
10 mmol of ethyl 4-(mercaptomethyl)-2-methyl-1,3-oxazole-5-carboxylate was dissolved in 100 ml of dried tetrahydrofuran, then 42 ml of the 0.5M SDBBA solution was gradually added with keeping the temperature at −30 to −20° C. After the adding, reaction was carried out for 4 hours at −20° C. Then 20 ml of wafer was added into the reaction system to stop the reaction and then an organic layer was separated. To the remaining water phase, sodium hydrogen carbonate was added until the pH of the water phase reached 8 to 9. The product was extracted and separated into an organic layer using ethyl acetate. This organic layer and the previously obtained organic layer were combined together and dried under sodium sulfate. The solvent was evaporated out and then the product was purified using a column separation with solvents of ethyl acetate and hexane, obtaining 4-(mercaptomethyl)-2-methyl-1,3-oxazole-5-carbaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08779086B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-92888ae2df684810ae2120e3c53724ec |
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| Source note | uspto-grants-2014_07 |
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