HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → Ethyl 2-allyl-2-(3-methoxyphenyl)butyrate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Ethyl 2-allyl-2-[3-(1-methyl-2-oxo-1,2-dihydroquinolin-6-ylmethoxy)phenyl]butyrate | HCID 57452573 | — |
| Product | Ethyl 2-allyl-2-(3-methoxyphenyl)butyrate | HCID 19091449 | — |
Reaction Steps
The ethyl 2-allyl-2-(3-hydroxyphenyl)butyrate used as a starting material was obtained using the procedures described in the portion of Example 1 which is concerned with the preparation of starting materials except that allyl bromide was used in place of ethyl iodide in the second alkylation step. The intermediate so obtained, ethyl 2-allyl-2-(3-methoxyphenyl)butyrate gave the following characteristic NMR signals: 0.76 (t, 3 H), 1.18 (t, 3 H), 2.05 (m, 2 H), 2.75 (m, 2 H), 3.80 (s, 3 H), 4.15 (q, 2 H), 5.15 (m, 2 H), 5.50 (m, 1 H), 6.80 (m, 3 H), 7.22 (m, 1 H). ##STR2##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05298511 |
| Source dataset | uspto-grants-1994_03 |
| ORD ID | ord-ddf3ee14de3944b1bfa61c1c8354cf89 |
| Source note | uspto-grants-1994_03 |