HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1577104Generated: October 26, 2026
Dimethyl Sulfoxide → 7-[2-Methoxyethylamino]-6-nitro-4-trifluoromethyl-1,3-benzodithiol-2-one
https://huagongshe.com/reaction/1577104
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Dimethyldithiocarbamic acid | HCID 6599 | — |
| Reactant | 3,5-Dinitro-4-[2-methoxyethyl-amino]-2-chlorobenzotrifluoride | HCID 20571868 | — |
| Product | 7-[2-Methoxyethylamino]-6-nitro-4-trifluoromethyl-1,3-benzodithiol-2-one | HCID 20571867 | — |
Reaction Steps
A solution of 9.5 g (0.053 mole) of N,N-dimethyldithiocarbamic acid (sodium salt dihydrate) in 25 ml of dimethyl sulfoxide is added dropwise at 20° C. in the course of 1 hour to a solution of 18 g (0.052 mole) of 3,5-dinitro-4-[2-methoxyethylamino]-2-chlorobenzotrifluoride in 160 ml of dimethyl sulfoxide, and the batch is stirred for 11/2 hours at room temperature. Stirring is then continued for 3 hours at 80° C. (internal temperature). For working up, the reaction mixture is poured on ice-water and extracted three times with ether. The combined ethereal phases are washed four times with water and three times with sodium chloride solution, died over sodium sulfate, filtered, and concentrated. The residue is recrystallised from ether, affording 7-[2-methoxyethylamino]-6-nitro-4-trifluoromethyl-1,3-benzodithiol-2-one with a melting point of 96°-98° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04287204 |
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| Source dataset | uspto-grants-1981_09 |
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| ORD ID | ord-899a82bfbd11442e8bdceb8ba82f972d |
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| Source note | uspto-grants-1981_09 |
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