Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylboraneHCID 7357—
ReactantSodium HydroxideHCID 14798—
ReactantN-[(E)-[3-[2-[4-(difluoromethoxy)phenyl]ethynyl]phenyl]methylideneamino]-4-methylbenzenesulfonamideHCID 59790336—
SolventTetrahydrofuranHCID 8028—
Product1-{[4-(Difluoromethoxy)phenyl]ethynyl}-3-propylbenzeneHCID 5743585689%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07423158B2
Source datasetuspto-grants-2008_09
ORD IDord-2afa4f797d6842c69a7d8f1808c9d185
Source noteuspto-grants-2008_09