HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Phenylethanol → Ethyl Acetoacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Phenylethanol | HCID 6054 | — |
| Reactant | 2,2-Diethoxyethylamine | HCID 69524 | — |
| Reactant | 3,4-Dimethoxyphenethyl alcohol | HCID 81911 | — |
| Product | Ethyl Acetoacetate | HCID 8868 | — |
| Product | 1-Methyl-1-isochromanacetic acid ethyl ester | HCID 54257169 | — |
Reaction Steps
In the same manner but replacing 3,4-dimethoxyphenethyl alcohol and aminoacetaldehyde diethyl acetal with equivalent amounts of phenethyl alcohol, Khafagy and Lambooy, cited above, and ethyl acetoacetate, respectively, 1-methyl-1-isochromanacetic acid ethyl ester, νmaxCDCl 3 1720 cm-1, nmr (CDCl 3) δ 1.5, 2.85, is obtained. Likewise, replacement with equivalent amounts of 1-naphthaleneethanol. M. Mousseron and Nguyen-Phuoc-Du. Bull. Soc. Chim. Fr., 91 (1948), and ethyl acetoacetate, gives 1,2-dihydro-4-methyl-4N-naphtho[2,1-c]pyran- 4-acetic acid ethyl ester, νmaxCHCl 3 1720 cm-1, nmr (CDCl 3) δ 1.5. Hydrogen bromide is a preferred acid catalyst for these latter two preparations.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04021451 |
| Source dataset | uspto-grants-1977_05 |
| ORD ID | ord-f6f2f0f17d0048dbbb3b0eabc4cacd94 |
| Source note | uspto-grants-1977_05 |