HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethanolamine → HCID 58912940, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethanolamine | HCID 8113 | — |
| Reactant | [4-(4-Benzyloxycarbonylaminobutyl)phenoxy]acetic acid ethyl ester | HCID 21031128 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 58912940 | HCID 58912940 | — |
Reaction Steps
A solution of [4-(4-benzyloxycarbonylaminobutyl)phenoxy]acetic acid ethyl ester 480 (0.3 g, 0.78 mmol), 2-(2-hydroxyethylamino)ethanol (0.15 m-L, 1.6 mmol), and ethanol (20 mL) was heated at 70° C. for 72 hours. The solvent was evaporated in vacuo. The residue was purified by flash chromatography (silica gel, dichloromethane/methanol, 100:5-1, v/v) to provide 490 (0.19 g, 100% based on the recovered starting material (0.13 g)) as a pale yellow solid. 1H NMR (300 MHz, CDCl3) δ 1.55 (m, 4H), 2.56 (t, 2H), 3.20 (q, 2H), 3.60 (m, 4H), 3.90 (m, 2H), 3.96 (m, 2H), 4.85 (s, 2H), 5.09 (s, 2H), 6.85 (d, 2H), 7.06 (d, 2H), 7.40 (m, 5H). m/z (ESI) 445.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07875619B2 |
| Source dataset | uspto-grants-2011_01 |
| ORD ID | ord-1da8ee88ea2040b2988a0c0f8de12bd5 |
| Source note | uspto-grants-2011_01 |