関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2-Methoxyethanol | HCID 8019 | — |
| 反応物 | Tributylphosphine | HCID 13831 | — |
| 反応物 | Methoxymethanol | HCID 62540 | — |
| 反応物 | 1,1'-(Azodicarbonyl)dipiperidine | HCID 73042 | — |
| 反応物 | Tert-butyl 2-(3-hydroxyquinolin-6-yl)acetate | HCID 57691372 | — |
| 溶媒 | Benzene | HCID 241 | — |
| 溶媒 | Hexane | HCID 8058 | — |
| 生成物 | Tert-butyl 2-(3-(2-methoxyethoxy)quinolin-6-yl)acetate | HCID 57690925 | — |
反応手順
To a suspension of tert-butyl 2-(3-hydroxyquinolin-6-yl)acetate (0.1 g, 0.4 mmol) in benzene (5 mL) was added 2-methoxyethanol (0.09 ml, 1 mmol) and tri-n-butylphosphine (0.1 ml, 0.6 mmol). The resulting mixture was cooled to 0° C. followed by adding 1.1′-(azodicarbonyl)dipiperidine (0.1 g, 0.6 mmol). After 10 min, ice bath was removed; the reaction mixture was warmed up to rt. After 2 h, TLC showed there still existed 50% starting material. More methoxymethanol (2 eq, 0.06 mL) was added. The reaction mixture was continued to stir for 20 h. Hexane was added to the reaction mixture and dihydro-ADDP separated out was filtered off. The filtrate was concentrated. The crude product was purified using SiO2 chromatography (Teledyne Isco RediSep®, P/N 68-2203-027, 40 g SiO2, hexane:acetone=85%:15%, Flow=40 mL/min) to afford the desired product as colorless liquid. MS m/z: 318.4 (M+H). Calc'd. for C18H23NO4—317.38.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US08212041B2 |
|---|
| 出典データセット | uspto-grants-2012_07 |
|---|
| ORD ID | ord-cd8b138c88e6416aa397fa9acf8950a8 |
|---|
| 出典メモ | uspto-grants-2012_07 |
|---|