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3-(benzyloxy)propyl Methanesulfonate → 2-(3-(3-(3-(Benzyloxy)propoxy)phenyl)propyl)isoindoline-1,3-dione
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 3-(benzyloxy)propyl Methanesulfonate | HCID 13709828 | — |
| 反応物 | 2-[3-(3-Hydroxyphenyl)propyl]isoindole-1,3-dione | HCID 58027542 | — |
| 生成物 | 2-(3-(3-(3-(Benzyloxy)propoxy)phenyl)propyl)isoindoline-1,3-dione | HCID 67317132 | — |
反応手順
Alkylation reaction of phenol 58 with methane sulfonic acid 3-benzyloxy-propyl ester gave 2-(3-(3-(3-(benzyloxy)propoxy)phenyl)propyl)isoindoline-1,3-dione as yellow oil. Yield (0.643 g, 44%): 1H NMR (400 MHz, DMSO-d6) δ 7.80-7.83 (m, 2H), 7.68-7.72 (m, 2H), 7.27-7.35 (m, 5H), 7.12-7.16 (m, 1H), 6.77 (d, J=7.6, 1H), 6.73 (s, 1H), 6.66 (d, J=8.0, 1H), 4.53 (s, 2H), 4.06 (t, J=6.0 Hz, 2H), 3.77 (t, J=6.2 Hz, 2H), 3.68 (t, J=5.0 Hz, 2H), 2.65 (t, J=7.8 Hz, 2H), 2.0-2.10 (m, 4H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09079825B2 |
| 出典データセット | uspto-grants-2015_07 |
| ORD ID | ord-65f624334ee34578bb65153d78bfc934 |
| 出典メモ | uspto-grants-2015_07 |