HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Propanoic acid, 2-bromo-2-methyl-, ethyl ester → 6-Methoxy-2-naphthaldehyde
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Propanoic acid, 2-bromo-2-methyl-, ethyl ester | HCID 11745 | — |
| Edukt | Ethyl 6-methoxy-2-naphthoate | HCID 226777 | — |
| Edukt | 6-Methoxynaphthalene-2-carbonitrile | HCID 349173 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Katalysator | Zinc | HCID 23994 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 6-Methoxy-2-naphthaldehyde | HCID 76991 | — |
Reaktionsschritte
6-methoxy-2-naphthaldehyde (substrate IIA) was synthesized from 6-methoxy-2-carbethoxynaphthalene, prepared from 6-methoxy-2-naphthonitrile, ethyl 2-bromoisobutyrate, and zinc dust as described by Horeau et al., 1947, Bull. Soc. Chim. Fr. 14:53-59. The keto-ester intermediate, mp 74°-76° C. (lit. 72.5-73.5° C.) was reduced to the corresponding secondary alcohol ester with sodium borohydride in ethanol at 4° C. and then thermally decomposed (Horeau et al. 1953, Compt. Rend. 236:826-8) to afford the final compound. The aldehyde was 25 purified either by zone sublimation or via the bisulfite adduct; mp 80°-81.5° C.; (lit. 79° C. Horeau et al., 1953, supra: lit. 81°-82° C. Gandhi et al., 1955 J. Chem. Soc., 2530).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05162203 |
| Quelldatensatz | uspto-grants-1992_11 |
| ORD ID | ord-cb80d53f8a0441b0bf973772abcbb211 |
| Quellennotiz | uspto-grants-1992_11 |