HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phthalimide → HCID 69412703, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phthalimide | HCID 6809 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diethyl azodicarboxylate | HCID 5462977 | — |
| Reactant | HCID 69413563 | HCID 69413563 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 69412703 | HCID 69412703 | — |
Reaction Steps
The phenylmethylalcohol compound (1.98 grams) (Scheme C, Compound C1) was dissolved in tetrahydrofuran (100 mL). Triphenylphosphine (1.84 grams), phthalimide (1.03 grams) and diethylazodicarboxylate (1.10 mL) were added to the mixture which was then stirred for 16 hours before being evaporated in vacuo. The residue was column chromatographed (silica gel) using a mobile phase of hexane-ethyl acetate 2:1 to give a N-[3-[[4-(4-chlorophenyl)-2-thiazolyl]methoxy]phenylmethyl]phthalimide (Scheme C, Compound C2). Mp 156.5–157.5° C.; MS 461 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07179808B2 |
| Source dataset | uspto-grants-2007_02 |
| ORD ID | ord-6cad1b2aa9b34e7da1cceb21a86b45c4 |
| Source note | uspto-grants-2007_02 |