HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2177310Generated: October 31, 2026
Triphenylphosphine → HCID 90418267, compound
https://huagongshe.com/reaction/2177310
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl azodicarboxylate | HCID 5363146 | — |
| Reactant | HCID 90418354 | HCID 90418354 | — |
| Reactant | HCID 90418635 | HCID 90418635 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 90418267 | HCID 90418267 | — |
Reaction Steps
Into a 25-mL round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed [5-bromo-3-(trifluoromethyl)-1,2-thiazol-4-yl]methanol (200 mg, 0.76 mmol, 1.00 equiv), methyl 3-(3,5-difluoro-4-hydroxyphenyl)propanoate (199 mg, 0.92 mmol, 1.20 equiv), PPh3 (401 mg, 1.53 mmol, 2.00 equiv), tetrahydrofuran (3 mL), DIAD (3.9 mg, 0.02 mmol, 2.00 equiv). The resulting solution was stirred overnight at 25° C. The reaction progress was monitored by TLC (ethyl acetate/petroleum ether=1:4). The resulting mixture was concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1:4). This resulted in 190 mg (51%) of methyl 3-(4-[[5-bromo-3-(trifluoromethyl)-1,2-thiazol-4-yl]methoxy]-3,5-difluorophenyl)propanoate as yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09067898B1 |
|---|
| Source dataset | uspto-grants-2015_06 |
|---|
| ORD ID | ord-b5a1bd16c7204c8fa2169ab29ed733bf |
|---|
| Source note | uspto-grants-2015_06 |
|---|