HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylpyridine-2-carbaldehyde → 2-(1-Hydroxy-1-cyclopropylmethyl)-4-methyl-pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylpyridine-2-carbaldehyde | HCID 10011894 | — |
| Reactant | HCID 178418630 | HCID 178418630 | — |
| Product | 2-(1-Hydroxy-1-cyclopropylmethyl)-4-methyl-pyridine | HCID 18799903 | 87% |
Reaction Steps
The Grignard reaction of 4-methyl-2-pyridinecarboxaldehyde (1.21 g, 10.0 mmol) and cyclopropylmagnesium bromide (24 ml, 15.0 mmol, 1.5 equiv., 1.6 ml/mmol) provided 1.42 g (87%) of 2-(1-hydroxy-1-cyclopropylmethyl)-4-methyl-pyridine. TLC (silica gel GF): Rf =0.21 acetone-methylene chloride (1:6). 1H NMR (CDCl3,TMS): δ 8.47 (d, 1H, J=5.08 Hz), 7.30 (s, 1H), 7.12 (d, 1H, J=5.14 Hz), 4.70 (brs, 1H), 4.16 (d, 1H, J=7.92 Hz), 2.47 (s, 3H), 1.26-1.12 (m, 1H), 0.74-0.57 (m, 4H). Mass Spectrum: M/Z (relative intensity %): 163 (34), 162 (51), 146 (51), 135 (70), 122 (100), 107 (57), 92 (98).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06043248 |
| Source dataset | uspto-grants-2000_03 |
| ORD ID | ord-5cdf56e0d1cf46f5870e6983eb53f917 |
| Source note | uspto-grants-2000_03 |