HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 3,5-Dichloro-2-hydroxy-4-(4-tert-butoxycarbonylmethylaminobutoxy)benzoic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | 4-Tert-butoxycarbonylmethylamino-1-butanol | HCID 10845828 | — |
| Reactant | Methyl 3,5-dichloro-2,4-dihydroxybenzoate | HCID 15489807 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3,5-Dichloro-2-hydroxy-4-(4-tert-butoxycarbonylmethylaminobutoxy)benzoic acid methyl ester | HCID 54319283 | 83.4% |
Reaction Steps
To a solution of 4-tert-butoxycarbonylmethylamino-1-butanol (3 g) and known 3,5-dichloro-2,4-dihydroxybenzoic acid methyl ester (3.85 g) in THF (80 ml) were added triphenylphosphine (4.26 g) and diisopropyl azodicarboxylate (3.2 ml) under ice-cooling, and the mixture was stirred for 16 hours. The reaction mixture was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (developing solvent: hexane/ethyl acetate=4/1 v/v) to give the title compound (5.2 g, yield 83%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06420561B1 |
| Source dataset | uspto-grants-2002_07 |
| ORD ID | ord-c87f8d0962944403ae905f1f035bc7b9 |
| Source note | uspto-grants-2002_07 |