化工社化工社 化学情報印刷レポート · 研究参考用
Triethylamine → alpha-D-Mannopyranose
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | alpha-Mannose phenylaminocyclobutenedione | HCID 86678081 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Water ethanol | HCID 19096565 | — |
| 生成物 | alpha-D-Mannopyranose | HCID 185698 | — |
反応手順
Nanoparticles DB052 (200 mg) were stirred up by ultrasounds for 30 minutes in ethanol (5 mL). α-mannose phenylaminocyclobutenedione derivatives (71 mg, 1.8 10−4 mol, structure here above) was dissolved in an ethanol/water mixture (10 ml, 3/2). The α-mannose phenylaminocyclobutenedione derivative solution was added dropwisely to the nanoparticle suspension. Triethylamine (500 μL) was added, and the suspension was stirred for 18 hours. After centrifugation, the nanoparticles were dispersed in water and centrifuged (3 cycles), then dispersed in ethanol and centrifugated (two cycles). Functionalized nanoparticles (DB069) were obtained (200 mg).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08709747B2 |
| 出典データセット | uspto-grants-2014_04 |
| ORD ID | ord-d956c0b2d6f44e7aad3939dd97a400b7 |
| 出典メモ | uspto-grants-2014_04 |