Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Chlorosulfonic acid | HCID 24638 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | N-(4-Bromobenzyl)-2,2-dimethoxyethanamine | HCID 59226241 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 6-Bromoisoquinoline | HCID 313681 | — |
Reaktionsschritte
To a stirred solution of N-(4-bromobenzyl)-2,2-dimethoxyethanamine (10 g, 0.037 mol) in CH2Cl2 (100 mL) was added ClSO3H (21.3 g, 0.18 mol) at −20° C. dropwise. The resulting reaction mixture was allowed to stir at 45° C. for 10 h. The resulting reaction mixture was diluted with CH2Cl2 and ice cold H2O, then neutralized with aqueous NaHCO3. The organic layer was separated and aqueous layer extracted with CH2Cl2. The combined organic layers were dried over Na2SO4 and concentrated at reduced pressure to get crude 6-bromoisoquinoline, which was purified by silica gel chromatography eluting with 5-15% EtOAc-hexanes to afford 6-bromoisoquinoline (0.9 g, 12%) as yellow liquid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09334269B2 |
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| Quelldatensatz | uspto-grants-2016_05 |
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| ORD ID | ord-64832c05b3cc49e5ac0d766a34e2b5bc |
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| Quellennotiz | uspto-grants-2016_05 |
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