HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402827Generated: October 25, 2026
4-Methylmorpholine → Methyl 3,5-dibromo-4-{[(phenylsulfanyl)carbonothioyl]oxy}benzoate
https://huagongshe.com/reaction/402827
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Phenyl Chlorodithioformate | HCID 592675 | — |
| Reactant | Methyl 3,5-dibromo-4-hydroxybenzoate | HCID 726975 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 3,5-dibromo-4-{[(phenylsulfanyl)carbonothioyl]oxy}benzoate | HCID 77230874 | 99.9% |
Reaction Steps
Methyl 3,5-dibromo-4-hydroxybenzoate (1000 mg, 3.23 mmol) was dissolved in THF (16 mL) and N-methylmorpholine (0.709 mL, 6.45 mmol) was added. The mixture was cooled to 0° C. and phenyl chlorodithioformate (0.549 mL, 3.87 mmol) was added. The mixture was warmed to room temperature and stirred overnight. The mixture was diluted with EtOAc and washed with water. The organic layer was dried over Na2SO4, filtered and concentrated. The residue was purified by silica gel chromatography (0-15% EtOAc/hexanes) to yield the title compound as a clear oil (1491 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08742110B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-719259b39ba4474b81d51115e00d21d3 |
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| Source note | uspto-grants-2014_06 |
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