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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 462485Generated: October 29, 2026

Methane → Ethanethioamide, N-(4-methoxy-3-methylphenyl)-

https://huagongshe.com/reaction/462485

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantPhosphorus sulfide (P2S5)HCID 14817—
ReactantHCID 4004288HCID 4004288—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
Solvent1,4-DioxaneHCID 31275—
ProductEthanethioamide, N-(4-methoxy-3-methylphenyl)-HCID 3034997—

Reaction Steps

185 g of 2-methyl-4-acetamino-anisole (prepared by procedures described by M. Heidelberg and W. A. Jacobs in J.A.C.S. 41 (1919) p. 1453), 100 ml of pyridine and 250 ml of anhydrous dioxane were poured into a 1 l. multi-neck flask mounted on an oil bath whose temperature was 100° C. After complete dissolution, 130 g of P2S5 were added thereto in small portions under stirring; after the addition, the solution thus obtained was stirred for another 45 minutes by maintaining the conditions of the reaction temperature. The reaction mixture was poured into a 5 l. of a very cold water solution of 45 g of NaOH; animal charcoal was added thereto and the whole stirred for 1 hour. After filtration, the solution was poured into a Keller flask, provided with a stirrer and externally cooled, cautiously acidified with concentrated HCl to pH=4-5, keeping the temperature lower than +5° C. After approximately 1 hour of stirring, the product, thus separated, was filtered with a Buchner and washed with water. The raw product was crystallized many times from ligroin in the presence of animal charcoal to reach a melting point of 88.5°-89° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04515888
Source datasetuspto-grants-1985_05
ORD IDord-f1587fe15e5d4ce39941047018da03e6
Source noteuspto-grants-1985_05