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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442977Generated: October 30, 2026

1,3-Propanediol → HCID 54020412, compound

https://huagongshe.com/reaction/442977

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-PropanediolHCID 10442—
ReactantTributylphosphineHCID 13831—
Reactant1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
ReactantHCID 54212462HCID 54212462—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 54020412HCID 5402041279.2%

Reaction Steps

To a solution of 3-(3-cyanophenylsulfonyloxy)-5-methylphenol (2.30 g, 8.0 mmol), as prepared in the preceding step, tri-n-butylphosphine (2.4 g, 12.0 mmol) and 1,3-propanediol (3.0 g, 40 mmol) in anhydrous tetrahydrofuran (50 mL) was added 1,1'-(azodicarbonyl)dipiperidine (3.0 g, 12.0 mmol). The mixture was stirred at ambient temperature overnight. Hexane (100 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 (10% ethyl acetate in dichloromethane) to give the title compound as a colorless oil (2.2 g, 79%). 1H-NMR (300 MHz, CDCl3) δ 8.13 (s, 1H), 8.10 (d, J=8.0 Hz, 1H), 7.95 (d, J=7.9 Hz, 1H), 7.71 (t, J=7.9 Hz, 1H), 6.65 (s, 1H), 6.40 (s, 1H), 6.37 (s, 1H), 4.02 (t, J=6.0 Hz, 2H), 3.82 (t, J=6.0 Hz, 2H), 2.26 (s, 3H), 2.00 (t, J=6.0 Hz, 2H), 1.67 (br s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05891909
Source datasetuspto-grants-1999_04
ORD IDord-af3661cbdbba492e819e6c41542d9dde
Source noteuspto-grants-1999_04