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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1367723Generated: October 25, 2026

Ethyl 6-bromohexanoate → Ethyl 17-(tetrahydropyran-2-yl-oxy)-heptadecanoate

https://huagongshe.com/reaction/1367723

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 6-bromohexanoateHCID 117544—
ReactantTetrahydropyran, 2-(11-iodoundecyloxy)-HCID 558999—
Reactant(S,S)-2,6-Bis(4-isopropyl-2-oxazolin-2-yl)pyridineHCID 688211—
CatalystZincHCID 23994—
Catalyst18-(p-Iodophenyl)octadecanolHCID 11655804—
CatalystDichloronickel;1,2-dimethoxyethaneHCID 15773433—
SolventDimethylacetamideHCID 31374—
Solvent(R,R)-2,6-Bis(4-isopropyl-2-oxazolin-2-yl)pyridineHCID 688213—
ProductEthyl 17-(tetrahydropyran-2-yl-oxy)-heptadecanoateHCID 6697014995%

Reaction Conditions

Temperature0 °C

Reaction Steps

From (77) and (36). Zinc powder (342 mg, 5.27 mmol) was dried at 70° C. for 30 min in a sealed tube, then DMA (2 ml) and solid 12 (45 mg, 0.18 mmol) were added. After stirring for 10 min, neat ethyl 6-bromohexanoate (0.63 ml, 3.52 mmol) was added and the reaction mixture was stirred in the sealed tube for 10 h at 75° C. In a 10-ml flask, NiCl2-glyme (52 mg, 0.23 mmol) and (R)-(i-Pr)-Pybox (or (S)-(i-Pr)-Pybox) (92 mg, 0.31 mmol) were dissolved in DMA (1.5 ml), cooled to 0° C. and solution of I(CH2)11OTHP 77 (896 mg, 2.34 mmol) in DMA (0.5 ml) was added. Then the solution of organozinc reagent 36 was added. The reaction mixture was stirred at 0° C. for 6 h and at room temperature for 6 h, then quenched by addition of aqueous NH4Cl, extracted with EtOAc, extract was dried over Na2SO4 and evaporated. The crude product was purified as in Method 1 to give compound 78 (888 mg, 95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893286B2
Source datasetuspto-grants-2011_02
ORD IDord-7e663649b5854a36b5a4de9c6acbe9d5
Source noteuspto-grants-2011_02