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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442910Generated: October 30, 2026

1,3-Propanediol → HCID 53991855, compound

https://huagongshe.com/reaction/442910

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-PropanediolHCID 10442—
ReactantTributylphosphineHCID 13831—
Reactant1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
ReactantHCID 11045855HCID 11045855—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 53991855HCID 5399185590%

Reaction Steps

To a solution of 3-(2,5-dichlorophenylsulfonyloxy)-5-methylphenol (642 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 ambient 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 (700 mg, 90%). 1H-NMR (300 MHz, CDCl3) δ 7.96 (s, 1H), 7.56 (s, 2H), 6.63 (s, 1H), 6.55 (s, 1H), 6.51 (s, 1H), 4.03 (t, J=6.0 Hz, 2H), 3.82 (m, 2H), 2.26 (s, 3H), 2.00 (m, 2H), 1.58 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05891909
Source datasetuspto-grants-1999_04
ORD IDord-03c4ebcf9b89470dba2b87b8166ed29a
Source noteuspto-grants-1999_04