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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1456858Generated: November 3, 2026

Methanol → HCID 10769106, compound

https://huagongshe.com/reaction/1456858

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 54443927HCID 54443927—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10769106HCID 1076910688%

Reaction Steps

To a mixture in THF (50 mL) of 4.4-bis(4-(2-quinolylmethoxy)phenyl)pentanoic acid 2-quinolylmethyl ester (2.1 g, 3 mmol), prepared as in Example 1, and sodium borohydride (380 mg, 10 mmol) was added dropwise methanol at 50°-55° C. and the mixture was stirred for 30 minutes. The mixture was cooled to room temperature, poured into water (50 mL) and acidified to pH 4. The resulting mixture was extracted with ethyl acetate, dried over MgSO4, filtered, and concentrated in vacuo. The residue was purified by chromatography on silica gel (methylene chloride-ethyl acetate 3:1) to afford 1.46 g (88%) of 4,4-bis(4-(2-quinolylmethoxy)phenyl)pentan-1-ol: 1H NMR (300 MHz, DMSO-d6) d 1.18 (m, 2H), 1.48 (s, 3H), 2.00 (m, 2H), 3.34 (m, 2H), 4.34 (t, 1H, J=6 Hz), 5.30 (s, 4H), 6.96 (d, 4H, J=9 Hz), 7.09 (d, 4H, J=9 Hz), 7.64 (m, 4H), 7.79 (m, 2H), 8.00 (t, 4H, J=8 Hz), 8.41 (d, 2H, J=8 Hz); MS (DCl--NH3) m/e 555 (M+H)+. Anal. Calc'd. for C37H34N2O3.0.5 H2O: C, 78.84; H, 6.44; N, 4.97. Found: C, 78.67; H, 5.95; N, 4.70.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05843968
Source datasetuspto-grants-1998_12
ORD IDord-d40cc56d0e8a4140b0daa1d3008aa058
Source noteuspto-grants-1998_12