HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389467Generated: October 30, 2026
Water → 3-Bromo-2-tert-butylsulfanyl-5-nitro-benzaldehyde
https://huagongshe.com/reaction/389467
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | tert-Butyl mercaptan | HCID 6387 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Bromo-2-fluoro-5-nitrobenzaldehyde | HCID 86662401 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Bromo-2-tert-butylsulfanyl-5-nitro-benzaldehyde | HCID 86662400 | 104.8% |
Reaction Steps
A mixture of 3-bromo-2-fluoro-5-nitro-benzaldehyde (1.0 g, 4 mmol), potassium carbonate (667 mg, 4.8 mmol) and 2-methyl-2-propanethiol (326 mg, 0.40 mL, 3.6 mmol) in dry DMF (5 mL) was heated at 110° C. in a sealed tube for 16 h. The reaction was cooled to RT, water was added, and the mixture extracted with dichloromethane (2×30 mL). The combined organic fractions were washed with water (3×15 mL), dried over sodium sulfate, filtered and concentrated to afford 1.2 g of the crude title compound, which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08378104B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-2c4fecd2afb640f0bd8d512cea9bed19 |
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| Source note | uspto-grants-2013_02 |
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