HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → [2-(2-Hydroxy-ethoxy)-ethyl]-carbamic acid anthracen-9-ylmethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Diglycolamine | HCID 13578 | — |
| Reactant | 9-Anthracenemethanol | HCID 73848 | — |
| Reactant | 4-Nitrophenyl chloroformate | HCID 82129 | — |
| Catalyst | Gold | HCID 23985 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | [2-(2-Hydroxy-ethoxy)-ethyl]-carbamic acid anthracen-9-ylmethyl ester | HCID 10315131 | — |
Reaction Steps
To a stirring slurry of 9-anthracenemethanol (10 g, 48 mmol) and 4-nitrophenyl chloroformate (13.6 g, 67.5 mmol) in 200 ml CH2Cl2 was added triethylamine (6.7 ml, 0.19 mol). The resulting gold colored solution was allowed to stir 16 hrs at room temperature. At this point, 2-(2-aminoethoxy)ethanol (14.4 ml, 0.144 mol) was added and stirring continued for another 24 hours. The CH2Cl2 reaction mixture was then washed with a 2% sodium hydroxide (w/w) solution until no p-nitrophenol was observed in the organic layer. The dichloromethane was dried with sodium sulfate, filtered, and evaporated under reduced pressure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07867726B2 |
| Source dataset | uspto-grants-2011_01 |
| ORD ID | ord-c0559f0ff65d4f29bdb383e3ad7971d8 |
| Source note | uspto-grants-2011_01 |