HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591440Generated: October 26, 2026
Tributylphosphine → (6-((1-Methyl-3-(trifluoromethyl)-1H-pyrazol-5-yl)methoxy)-4-(trifluoromethyl)-1-benzothiophen-3-yl)acetic acid
https://huagongshe.com/reaction/591440
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tributylphosphine | HCID 13831 | — |
| Reactant | 1,1'-(Azodicarbonyl)dipiperidine | HCID 73042 | — |
| Reactant | (1-Methyl-3-(trifluoromethyl)-1H-pyrazol-5-yl)methanol | HCID 58456726 | — |
| Reactant | Methyl 2-[6-hydroxy-4-(trifluoromethyl)benzo[b]thiophen-3-yl]acetate | HCID 89767967 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (6-((1-Methyl-3-(trifluoromethyl)-1H-pyrazol-5-yl)methoxy)-4-(trifluoromethyl)-1-benzothiophen-3-yl)acetic acid | HCID 89768892 | 70.7% |
Reaction Steps
To a mixture of methyl(6-hydroxy-4-(trifluoromethyl)-1-benzothiophen-3-yl)acetate (60 mg) and THF (dry) (3 mL) were added (1-methyl-3-(trifluoromethyl)-1H-pyrazol-5-yl)methanol (37.2 mg), ADDP (62.6 mg) and tri-n-butylphosphine (0.071 mL) at room temperature. The mixture was stirred at room temperature for 12 h. The insoluble material was removed by filtration, and the filtrate was concentrated in vacuo. The residue was purified by silica gel column chromatography (EtOAc/hexane). To the mixture of the crude material and THF (1 mL) was added 1N NaOH (1 mL) at room temperature for 12 h. The mixture was neutralized with 1N HCl at 0° C. and extracted with EtOAc. The organic layer was separated, washed successively with water and brine, dried over MgSO4 and concentrated in vacuo. The solid was crystallized from EtOAc-hexane to give the title compound (64.0 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09238639B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-4951a2f81ee34efc9ef0ce721aae98d6 |
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| Source note | uspto-grants-2016_01 |
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