HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1455770Erstellt: 26. Oktober 2026
Sodium Methoxide → 2-Chloro-5-[(5-isopropyl-2-methylphenoxy)methyl]-4-methoxy-6-methylpyrimidine
https://huagongshe.com/reaction/1455770
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Sodium Methoxide | HCID 10942334 | — |
| Edukt | 2,4-Dichloro-5-(5-isopropyl-2-methyl-phenoxymethyl)-6-methyl-pyrimidine | HCID 57531442 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | 2-Chloro-5-[(5-isopropyl-2-methylphenoxy)methyl]-4-methoxy-6-methylpyrimidine | HCID 57531406 | — |
Reaktionsschritte
A solution of ˜70% 2,4-dichloro-5-(5-isopropyl-2-methyl-phenoxymethyl)-6-methyl-pyrimidine (2.64 g, ˜5.68 mmol) is cooled to −5° C. under nitrogen with magnetic stirring. A 0.5 M solution of NaOMe in MeOH (11.4 mL) is added in rapid dropwise fashion. After 1 h, reaction is complete based on LC/MS analysis. The reaction mixture is evaporated at reduced pressure, diluted with DCM (15 mL), filtered and evaporated to obtain a pale yellow oil consisting of an isomeric mixture of mono-methoxy adducts. Purification on silica gel (10-60% EtOAc/Hexanes) provides a colorless oil containing the desired isomer. (first to elute) plus impurity from the starting material. 1H NMR (400 MHz, CDCl3) δ 7.06 (d, J=8 Hz, 1H), 6.82 (s, 1H), 6.78 (d, J=8 Hz, 1H), 5.05 (s, 2H), 4.04 (s, 3H), 2.80 (m, 1H), 2.55 (s, 3H), 2.13 (s, 3H), 1.26 (d, J=6.8 Hz, 6H); LC-MS found 321.1 (MH+), rt=1.73 min, Method 2.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07482350B2 |
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| Quelldatensatz | uspto-grants-2009_01 |
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| ORD ID | ord-70b8183f80354f429df3021a5074cb9b |
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| Quellennotiz | uspto-grants-2009_01 |
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