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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 846189Generated: October 26, 2026

Tetrahydrofuran → Tert-butyl 3-hydroxy-3-[2-(8-phenyloctyl)phenyl]propionate

https://huagongshe.com/reaction/846189

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactanttert-Butyl bromoacetateHCID 79177—
ReactantDiethyl aluminum chlorideHCID 16686102—
Reactant2-(2-Dodecylphenyl)-2-[[1-(3-carboxypropyl)-5-tetrazolyl]thio]acetic acidHCID 19880382—
CatalystZincHCID 23994—
Catalystcopper(I) bromideHCID 24593—
SolventHexaneHCID 8058—
ProductTert-butyl 3-hydroxy-3-[2-(8-phenyloctyl)phenyl]propionateHCID 15617420—

Reaction Conditions

Temperature-20 °C

Reaction Steps

A solution of diethlaluminum chloride (0.0082 moles, 8.2 ml) in hexane was added to a slurry of zinc dust (0.0111 mol: 0.7248 g) and a catalytic amount of copper (I) bromide (0.004 mol; 0.0585 g) in anhydrous tetrahydrofuran (40 ml) while stirring under argon at 20° C. the resulting mixture was then cooled to -20° C. in an ice-methanol bath. A solution of t-butyl bromoacetate (0.0082 mol; 1.32 ml) and 2-(8-phenyloctyl)benzylaldehyde of Example 5(a) or (b) (0.0082 moles; 2.3969 g) in anhydrous tetrahydrofuran was added slowly over 60 min. The reaction was stirred overnight and was permitted to warm up slowly to room temperature. The mixture was filtered to remove zinc, concentrated, and azeotroped with methylene chloride. The resulting oil was then chromatographed on silica using 5% ethyl acetate in hexane with 0.5% formic acid to yield the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05135938
Source datasetuspto-grants-1992_08
ORD IDord-6f16b235f1344b378bd1cdc68173c15c
Source noteuspto-grants-1992_08