HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 9-Fluorenylmethyl carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Phenol | HCID 996 | — |
| Reactant | Anisomycin | HCID 253602 | — |
| Reactant | 9-Fluorenylmethyl succinimide | HCID 22323418 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 9-Fluorenylmethyl carbamate | HCID 736301 | — |
Reaction Steps
Phenol 21 in FIG. 40 was synthesized as follows. Anisomycin 19 (0.5 g 1.88 mmol) was suspended in 15 mL of acetonitrile. 9-Fluorenylmethyl succinimide (0.762 g 2.26 mmol) was added to the suspension. Upon addition, all solid dissolved. After stirring for 16 hours at room temperature, water was added to the reaction solution, and it was extracted with ethyl acetate. The organics were combined and dried over sodium sulfate. After filtration and concentration, purification was accomplished by column chromatography using 3:1 hexanes:ethyl acetate as the mobile phase. This gave 9-fluorenylmethyl carbamate 20 as foam in quantitative yields (0.916 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06947845B2 |
| Source dataset | uspto-grants-2005_09 |
| ORD ID | ord-8f1f127110d14f27b8b6d2ef0c764dfe |
| Source note | uspto-grants-2005_09 |