HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442895Generated: October 25, 2026
1,3-Propanediol → 3-[5-Methyl-3-(2-trifluoromethylphenylsulfonyloxy)phenoxy]propanol
https://huagongshe.com/reaction/442895
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,3-Propanediol | HCID 10442 | — |
| Reactant | Tributylphosphine | HCID 13831 | — |
| Reactant | 1,1'-(Azodicarbonyl)dipiperidine | HCID 73042 | — |
| Reactant | 5-Methyl-3-(2-trifluoromethylphenylsulfonyloxy)phenol | HCID 22722649 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 3-[5-Methyl-3-(2-trifluoromethylphenylsulfonyloxy)phenoxy]propanol | HCID 22722497 | 95.4% |
Reaction Steps
To a solution of 5-methyl-3-(2-trifluoromethylphenylsulfonyloxy)phenol (665 mg, 2.0 mmol), as prepared in the preceding step, tri-n-butylphosphine (607 mg, 3.0 mmol), and 1,3-propanediol (760 mg, 10 mmol) in anhydrous tetrahydrofuran (20 mL) was added 1,1'-(azodicarbonyl)dipiperidine (757 mg, 3.0 mmol). The mixture was stirred at room temperature overnight. Hexane (30 mL) was added to the mixture, and the precipitates were removed by filtration. The filtrate was evaporated in vacuo, and the residue was purified by flash column chromatography (2:1 hexane/ethyl acetate) to give the title compound as a colorless oil (745 mg, 94%). 1H-NMR (300 MHz, CDCl3) δ 8.13 (d, J=7.2 Hz, 1 H), 7.99 (d, J=7.2 Hz, 1 H), 7.80 (t, J=7.6 Hz, 1 H), 7.70 (t, J=7.3 Hz, 1 H), 6.63 (s, 1 H), 6.48 (s, 1 H), 6.46 (s, 1 H), 4.02 (t, J=6.0 Hz, 2 H), 3.81 (m, 2 H), 2.25 (s, 3 H), 1.99 (m, 2 H), 1.61 (s, 1 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05891909 |
|---|
| Source dataset | uspto-grants-1999_04 |
|---|
| ORD ID | ord-0bdfce39e4234cb984828eded1938b34 |
|---|
| Source note | uspto-grants-1999_04 |
|---|