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1-Dodecanol → [1,1':3',1"-Terphenyl]-2'-yl[(dodecyloxy)sulfonyl]carbamate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1-Dodecanol | HCID 8193 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | [1,1':3',1"-Terphenyl]-2'-yl(chlorosulfonyl)carbamate | HCID 10572313 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | [1,1':3',1"-Terphenyl]-2'-yl[(dodecyloxy)sulfonyl]carbamate | HCID 15233160 | 42.5% |
反応手順
A solution of [1,1':3',1"-terphenyl]-2'-yl (chlorosulfonyl)carbamate (5.0 g, 12.9 mmoles) in 75 mL THF was added dropwise to a solution of n-dodecyl alcohol (2.4 g, 12.9 mmoles) and triethylamine (1.3 g, 12.9 mmoles) in 100 mL THF at ~15° C. under an atmosphere of N2. The mixture was allowed to warm to room temperature for 16 hours, then concentrated in vacuo and partitioned between H2O and EtOAc. The EtOAc layer was dried with MgSO4 and evaporated to give a white solid. Chromatography (SiO2, 10% EtOAc/hexanes) gave 2.95 g of the title compound, mp 124°-126° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05245068 |
| 出典データセット | uspto-grants-1993_09 |
| ORD ID | ord-77906ee1bea24ed3b1e739a1dc11b691 |
| 出典メモ | uspto-grants-1993_09 |