HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730952Generated: October 28, 2026
Formic Acid → methyl (3S)-3-hydroxy-3-(thiophen-2-yl)propanoate
https://huagongshe.com/reaction/730952
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Triethylammonium formate | HCID 11084032 | — |
| Reactant | Methyl 2-oxo-3-(2-thienyl)propionate | HCID 20277529 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | methyl (3S)-3-hydroxy-3-(thiophen-2-yl)propanoate | HCID 10397541 | — |
Reaction Steps
In a 1 l multinecked flask equipped with a sparging stirrer, reflux condenser and internal thermometer, an HCOOH/Et3N mixture (molar ratio 1:1) is prepared by gradually adding 41 ml of HCOOH dropwise within 20 min to 152 ml of Et3N with stirring and ice cooling. 190 g of methyl 2-oxo-3-(2-thienyl)propionate are added to this biphasic mixture, the homogeneous yellow solution is admixed with 0.1 l of dichloromethane and the entire mixture is degassed by passing through argon for 20 min. It is heated to 36° C. and the dark red catalyst solution is added all at once to the reaction mixture with vigorous stirring. Stirring is effected at 800 rpm while passing argon through the reaction mixture for 14 h.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07582776B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-6c96bfe041bd4053b8dc9a3953f3cccc |
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| Source note | uspto-grants-2009_09 |
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