HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389475Generated: October 30, 2026
Water → 3-Bromo-2-(tert-butylthio)-4-iodobenzaldehyde
https://huagongshe.com/reaction/389475
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-4-iodobenzaldehyde | HCID 86662403 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Bromo-2-(tert-butylthio)-4-iodobenzaldehyde | HCID 86662404 | 64% |
Reaction Steps
A mixture of 3-bromo-2-fluoro-4-iodo-benzaldehyde (1.3 g, 4.0 mmol), potassium carbonate (0.66 g, 4.7 mmol), and 2-methylpropane-2-thiol (0.53 mL, 4.7 mmol) in dry DMF (2 mL) was heated at 80° C. in a sealed tube for 16 h. The reaction mixture was cooled to RT, water was added, and the mixture was extracted with dichloromethane (2×30 mL). The combined organic fractions were washed with water (60 mL), dried over sodium sulfate, filtered, and concentrated. Purification of the residue by column chromatography (5% ethyl acetate:hexanes) afforded 1.0 g (64%) of the title compound. 1H NMR (300 MHz, CDCl3): δ 1.30 (s, 9H), 7.54 (d, J=8.1 Hz, 1H), 7.87 (d, J=8.1 Hz, 1H), 10.29 (s, 1H).
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-3df3a2e646dd4600a47f956f67291a05 |
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| Source note | uspto-grants-2013_02 |
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