HuagongsheHuagongshe Chemistry Print Report · For research reference only
{2-[2-(2-{2-[2-(4-{2-[2-(2-{2-[2-(9H-fluoren-9-yl-methoxycarbonylamino)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-ethoxy}-phenoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-ethoxy}acetic acid tert-butyl ester → {2-[2-(2-{2-[2-(4-{2-[2-(2-{2-[2-(9H-fluoren-9-yl-methoxycarbonylamino)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-ethoxy}-phenoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-ethoxy}acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | {2-[2-(2-{2-[2-(4-{2-[2-(2-{2-[2-(9H-fluoren-9-yl-methoxycarbonylamino)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-ethoxy}-phenoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-ethoxy}acetic acid tert-butyl ester | HCID 67089303 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | {2-[2-(2-{2-[2-(4-{2-[2-(2-{2-[2-(9H-fluoren-9-yl-methoxycarbonylamino)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-ethoxy}-phenoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-ethoxy}acetic acid | HCID 67089203 | 96% |
Reaction Steps
To Compound 29 (196 mg, 0.25 mmol), 5% hydrated trifluoroacetic acid (1.5 ml) was added at room temperature; this was followed by stirring for 5 minutes. Toluene (about 1 ml) was added; after concentration under reduced pressure, the concentrate was purified by silica gel column chromatography (Yamazen YFLC Gel, eluent; chloroform containing 3% methanol-ethyl acetate solution containing 10% methanol) to yield Compound 30 (colorless oil 175 mg, 96%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07919653B2 |
| Source dataset | uspto-grants-2011_04 |
| ORD ID | ord-86224fce6c754ef2a829ac384c85c626 |
| Source note | uspto-grants-2011_04 |