HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 549909Generated: October 30, 2026
Tributylphosphine → (Z)-{4-[3-(4-iodo-phenyl)-3-phenyl-allyloxy]-2-methyl-phenoxy}-acetic acid methyl ester
https://huagongshe.com/reaction/549909
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tributylphosphine | HCID 13831 | — |
| Reactant | 1,1'-(Azodicarbonyl)dipiperidine | HCID 73042 | — |
| Reactant | Methyl 2-(4-hydroxy-2-methylphenoxy)acetate | HCID 23549552 | — |
| Reactant | HCID 67146681 | HCID 67146681 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (Z)-{4-[3-(4-iodo-phenyl)-3-phenyl-allyloxy]-2-methyl-phenoxy}-acetic acid methyl ester | HCID 67146661 | — |
Reaction Steps
To a solution of (Z)-3-(4-Iodo-phenyl)-3-phenyl-prop-2-en-1-ol (756 mg, 2.249 mmol) in dry tetrahydrofuran (40 mL) was added tributylphosphine (0.61 ml, 3.37 mmol). The mixture was cooled to 0° C. and added 1,1′-(azodicarbonyl)dipiperidine (850 mg, 3.37 mmol) and after 10 min (4-Hydroxy-2-methyl-phenoxy)-acetic acid methyl ester (485 mg, 2.47 mmol) was added. After 1.5 hr at 0° C. the reaction was allowed to warm up to ambient temperature and stirred overnight. The reaction mixture was added silica gel Fluka 60 (10 g) and evaporated in vacuo. The residue was purified by ISCO combiflash 16 (silica gel, DCM/MeOH 90:10) giving (Z)-{4-[3-(4-iodo-phenyl)-3-phenyl-allyloxy]-2-methyl-phenoxy}-acetic acid methyl ester as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07943613B2 |
|---|
| Source dataset | uspto-grants-2011_05 |
|---|
| ORD ID | ord-0fb83c0c177e4fcfb3ca4e7384fb89a9 |
|---|
| Source note | uspto-grants-2011_05 |
|---|