HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 372213Generated: October 29, 2026
Methanethiol → Methyl 2-methoxy-6-(methylthio)-nicotinate
https://huagongshe.com/reaction/372213
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanethiol | HCID 878 | — |
| Reactant | Methyl 6-chloro-2-methoxynicotinate | HCID 10560015 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 2-methoxy-6-(methylthio)-nicotinate | HCID 20328808 | — |
Reaction Steps
To 10 ml of a 1 N methanolic sodium methoxide solution are added dropwise 3 ml of a 3.5 N methanolic methylmercaptan solution. To the resultant methylmercaptide solution is added a solution of 2.01 g (0.01 mole) of methyl 2-methoxy-6-chloronicotinate (cf. Example 6 a)) in 30 ml of methanol. The reaction mixture is refluxed for 5 hours and the solvent is thereafter evaporated in vacuo. The residue is treated with 30 ml of saturated potassium carbonate solution and 150 ml of methylene chloride and separated in a separating funnel. The methylene chloride solution is dried over sodium sulphate and subsequently evaporated to dryness in vacuo. The crystallised residue is recrystallised from pentane and yields the methyl 2-methoxy-6-(methylthio)-nicotinate with a melting point of 71°-75° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04089960 |
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| Source dataset | uspto-grants-1978_05 |
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| ORD ID | ord-e14b28e3b0f841968c9aa89ac9d3dd52 |
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| Source note | uspto-grants-1978_05 |
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