HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 559776Generated: October 30, 2026
Tert-Butanesulfinamide → HCID 59278446, compound
https://huagongshe.com/reaction/559776
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tert-Butanesulfinamide | HCID 3382465 | — |
| Reactant | 6-Bromo-3-pyridinecarboxaldehyde | HCID 11769234 | — |
| Catalyst | Titanium isopropoxide | HCID 11026 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | HCID 59278446 | HCID 59278446 | — |
Reaction Steps
A mixture of 6-bromo-pyridine-3-carbaldehyde (1.0 g, 5.38 mmol), 2-methylpropane-2-sulfinamide (715 mg, 5.90 mmol) and titanium (IV) isopropoxide (2.5 mL, 8.53 mmol) in dichloroethane (10 mL) was warmed at 110° C. in the microwave for 15 minutes. The reaction was monitored by TLC (ethyl acetate-hexanes 2:8). The mixture was diluted with dichloromethane (100 mL) and water (5 mL) was added. The mixture was stirred for 10 minutes and then dried over magnesium sulfate. The crude material was purified by silica gel chromatography eluting with a gradient of 0-20% ethyl acetate in hexanes to afford 2-methyl-propane-2-sulfinic acid 1-(6-bromo-pyridin-3-yl)-meth-(E)-ylideneamide
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08063065B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-6208459bc42c40a0996f2c9896617a93 |
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| Source note | uspto-grants-2011_11 |
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