HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2358445Generated: October 30, 2026
Water → methyl 3-isothiocyanatothiophene-2-carboxylate
https://huagongshe.com/reaction/2358445
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Thiophosgene | HCID 10040 | — |
| Reactant | HCID 22256629 | HCID 22256629 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | methyl 3-isothiocyanatothiophene-2-carboxylate | HCID 2777461 | — |
Reaction Steps
Thiophosgene (1.1 mL, 1.1 eq) is added dropwise to a solution cooled down to 0° C. of 3-amino-2-thiophenecarboxylate (2 g, 1 eq) and triethylamine (3.9 g, 3 eq in tetrahydrofuran (100 ml). The mixture is stirred for 15 min at 0° C. then water (70 ml) and diethyl ether (150 ml) are added. After decantation and extractions, the organic phases are combined, washed with salt water, dried over Na2SO4 then concentrated under reduced pressure at 40° C. Purification of the residue by flash chromatography on silica gel (eluent: heptane 100% to heptane/ethyl acetate 7:3) produces the expected compound in the form of a beige powder (2.15 g, 85% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07763725B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-33d38eba3ae2445e9b16b10b66c16622 |
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| Source note | uspto-grants-2010_07 |
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