HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 846015Generated: October 30, 2026
Carbon Dioxide → 2-Chloro-4-fluoro-5-isothiocyanato-thiolbenzoic acid (methoxycarbonylmethyl) ester
https://huagongshe.com/reaction/846015
Participants
| Role | Name | HCID | Charge |
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| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Thiophosgene | HCID 10040 | — |
| Reactant | Calcium Carbonate | HCID 10112 | — |
| Reactant | 5-Amino-2-chloro-4-fluoro-thiolbenzoic acid (methoxycarbonylmethyl) ester | HCID 86746023 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Chloro-4-fluoro-5-isothiocyanato-thiolbenzoic acid (methoxycarbonylmethyl) ester | HCID 86746025 | — |
Reaction Steps
A solution of 3.8 g of the 5-amino-2-chloro-4-fluoro-thiolbenzoic acid (methoxycarbonylmethyl) ester obtained in accordance with Example P2 in 100 ml of dichloromethane is added dropwise at 25°-30° C. to a suspension of 6 g of calcium carbonate, 4 ml of thiophosgene, 20 ml of dichloromethane and 20 ml of water. After the evolution of carbon dioxide has ceased, the mixture is stirred for 18 hours at room temperature. After filtration and washing with water, the organic phase is separated off, dried over sodium sulfate and then concentrated by evaporation, yielding 4.8 g of 2-chloro-4-fluoro-5-isothiocyanato-thiolbenzoic acid (methoxycarbonylmethyl) ester in the form of an oil which is used in the next reaction step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05135562 |
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| Source dataset | uspto-grants-1992_08 |
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| ORD ID | ord-8ca9c1d976dc4be191799f94c561a7dc |
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| Source note | uspto-grants-1992_08 |
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