HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → 5-(9-(9-Fluorenylmethyloxycarbonyl)aminoxanthen-2-oxy)valeric Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Pentanoic acid, 5-[(9-hydroxy-9H-xanthen-2-yl)oxy]- | HCID 10734020 | — |
| Reactant | HCID 178514243 | HCID 178514243 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 5-(9-(9-Fluorenylmethyloxycarbonyl)aminoxanthen-2-oxy)valeric Acid | HCID 11800482 | — |
Reaction Steps
A solution of p-toluenesulfonic acid (0.15 g, 0.8 mmol) in glacial acetic acid (3 mL) was added dropwise at 25° C. over 15 minutes to a well-stirred suspsension of 5-(9-hydroxy-xanthen-2-oxy)valeric acid (2.0 g, 6.4 mmol) prepared as described above and Fmoc-amide (1.84 g, 8.2 mmol) in glacial acetic acid (50 mL). This mixture was stirred continuously and then filtered after 3 hours to collect a white solid which was washed with water (3×20 mL) and ehtyl ether (3×20 mL). The solid was dried in vacuo over P2O5 at 25° C. Yield: 2.35 g(61%, m.p. 210-211° C., Rf : 0.53 EtOAc/MeOh 5:1. NMR data and elemental analysis in accordance with structure. ##STR12##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05306562 |
| Source dataset | uspto-grants-1994_04 |
| ORD ID | ord-9bd3db620f2244e9b21dadf62e992355 |
| Source note | uspto-grants-1994_04 |