HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 859933Generated: October 29, 2026
Hydrochloric Acid → HCID 68410542, compound
https://huagongshe.com/reaction/859933
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | HCID 86612013 | HCID 86612013 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | HCID 68410542 | HCID 68410542 | 41% |
Reaction Steps
60.0 g (208 mmol) of ethyl 2-(2-chloro-6-fluorophenyl)malonate and 19.0 g (249 mmol) of thiourea were heated for 2.5 hours at 150° C. in 77 g (416 mmol) of n-tributylamine. Most of the ethanol formed was distilled off. 180 ml of an aqueous solution of 24.9 g (623 mmol) of NaOH were added to the reaction mixture once it had cooled down. After the aqueous phase had been treated with 50 ml of cyclohexane and stirred for approximately 30 minutes, it was separated off, treated with 35.4 g (142 mmol) of methyl iodide and stirred for approximately 16 hours at approximately 20 to 25° C. After acidification with dilute HCl solution and stirring for approximately 30 minutes, the precipitate was filtered off washing with water and drying gave 16.7 g of the title compound as white crystals of m.p. 250° C. (decomp.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07153860B2 |
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| Source dataset | uspto-grants-2006_12 |
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| ORD ID | ord-5f79d6e605c44837b694a62ed130dcbc |
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| Source note | uspto-grants-2006_12 |
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