HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30553Generated: October 25, 2026
Water → 1-{[4-(Difluoromethoxy)phenyl]ethynyl}-3-propylbenzene
https://huagongshe.com/reaction/30553
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Triethylborane | HCID 7357 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N-[(E)-[3-[2-[4-(difluoromethoxy)phenyl]ethynyl]phenyl]methylideneamino]-4-methylbenzenesulfonamide | HCID 59790336 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-{[4-(Difluoromethoxy)phenyl]ethynyl}-3-propylbenzene | HCID 57435856 | 89% |
Reaction Steps
A mixture of N′-[(1E)-(3-{[4-(difluoromethoxy)phenyl]ethynyl}phenyl)methylene]-4-methylbenzenesulfonohydrazide (0.67 mg, 1.52 mmol) in THF was treated with triethyl borane (1.0 M in THF, 1.52 mL, 1.52 mmol), stirred for 2 minutes, treated with NaOH (2.5 N, 0.61 mL, 1.52 mmol), refluxed for 2 hours, cooled to room temperature, poured into water and extracted with EtOAc. The organic extracts were combined, dried over MgSO4 and concentrated in vacuo. The resultant residue was purified on silica gel (ISCO) using hexanes/EtOAc (50/1) as the eluting solvents to give 1-{[4-(difluoromethoxy)phenyl]ethynyl}-3-propylbenzene as a clear oil (386 mg, 89% yield), MS m/e (M+H)+ 286; 1H NMR (400 MHz, DMSO-d6) 0.85 (t, J=7.32 Hz, 3H), 1.57 (m, 2H), 2.6 (t, J=7.32 Hz, 2H), 7.2 (m, 3H), 7.35-7.45 (m, 4H), 7.58 (d, J=8.79 Hz, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07423158B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-2afa4f797d6842c69a7d8f1808c9d185 |
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| Source note | uspto-grants-2008_09 |
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