HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2176336Generated: October 30, 2026
Ethanol → Ethyl N-phenylbenzenecarboximidothioate
https://huagongshe.com/reaction/2176336
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Benzenecarbothioamide, N-phenyl- | HCID 668263 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl N-phenylbenzenecarboximidothioate | HCID 13377974 | — |
Reaction Steps
First, 3.2 g of sodium ethoxide, 10 g of N-phenylthiobenzamide, and 60 mL of ethanol were put in a 300 mL three-neck flask, and this mixed solution was stirred at room temperature for 1 hour. Then, 3.7 mL of iodoethane was added to this mixed solution, and heated and stirred at 60° C. for 6 hours to be reacted. After the reaction, ethanol was distilled off under a reduced pressure to give a brown oily substance. This oily substance was dissolved in dichloromethane, and washed with water and then a saturated aqueous solution of sodium hydrogen carbonate. After the washing, anhydrous magnesium sulfate was added to the resulting organic layer for drying. The resulting mixture was subjected to gravity filtration, and the filtrate was concentrated, so that N-[(ethylsulfanyl)phenylmethylidene]aniline was prepared (a brown oily substance, crude yield: 110%). The synthetic scheme of Step 1 is shown by (a-5).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09065061B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-85c4f829e8c847ae83269f638e7a2c5d |
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| Source note | uspto-grants-2015_06 |
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