HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 572676Generated: October 26, 2026
Triacetoxyperiodinane → 6-Bromo-2-methylpyrimidine-4-carbaldehyde
https://huagongshe.com/reaction/572676
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triacetoxyperiodinane | HCID 159087 | — |
| Reactant | (6-Bromo-2-methylpyrimidin-4-yl)methanol | HCID 86675898 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-Bromo-2-methylpyrimidine-4-carbaldehyde | HCID 86675929 | 74.1% |
Reaction Steps
To a cold solution of (6-bromo-2-methylpyrimidin-4-yl)methanol (15 g, 73.9 mmol, Preparation #4) in DCM (300 mL) was added Dess-Martin periodinane (47.0 g, 111 mmol). The resulting suspension was allowed to warm to RT and stirred for about 2 h. The reaction mixture was re-cooled to about 0° C., quenched with sodiumthiosulphate solution (200 mL) and stirred vigorously for about 30 min. The organic layer was separated and washed successively with saturated sodium bicarbonate (2×200 mL), water (1×200 mL) and brine (1×200 mL). The organic layer was dried over sodium sulphate and concentrated under reduced pressure to afford 6-bromo-2-methylpyrimidine-4-carbaldehyde 11 g (74.1%), 1H NMR (400 MHz, DMSO) δ: 9.88 (s, 1H), 7.96 (s, 1H), 2.73 (s, 3H), IR Neat 1720 (C═O) cm−1
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09029409B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-fbf16991433a4b92958de7b716a0c201 |
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| Source note | uspto-grants-2015_05 |
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