HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tributylphosphine → HCID 86591573, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tributylphosphine | HCID 13831 | — |
| Reactant | 1,1'-(Azodicarbonyl)dipiperidine | HCID 73042 | — |
| Reactant | Benzeneacetic acid, 4-hydroxy-, methyl ester | HCID 518900 | — |
| Reactant | HCID 86591570 | HCID 86591570 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86591573 | HCID 86591573 | 100.2% |
Reaction Steps
To a mixture of 4-[methyl(4-phenyl-2-thiazolyl)aminomethyl]benzyl alcohol (1.00 g), methyl 2-(4-hydroxyphenyl)acetate (643 mg), tributylphosphine (1.30 g) and tetrahydrofuran (30 mL) was added 1,1′-(azodicarbonyl)dipiperidine (1.62 g) at room temperature and the mixture was stirred for 16 hrs. The precipitated crystals were filtered off. The filtrate was concentrated and the residue was subjected to silica gel column chromatography to give methyl 4-[4-[methyl(4-phenyl-2-thiazolyl)aminomethyl]benzyloxy]phenylacetate (1.48 g, quantitative) as a yellow oil from a fraction eluted with ethyl acetate-hexane (1:4, v/v).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07238716B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-0248939543da42b78e24e6daaf260534 |
| Source note | uspto-grants-2007_07 |