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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1675786Generated: October 31, 2026

2-(2-Bromoethoxy)tetrahydro-2H-pyran → HCID 59279574, compound

https://huagongshe.com/reaction/1675786

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(2-Bromoethoxy)tetrahydro-2H-pyranHCID 86621—
ReactantOxindoleHCID 321710—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59279574HCID 59279574—

Reaction Steps

Potassium tert-butoxide (10.1 g, 90.1 mmol) was added to a solution of oxindole (3.00 g, 22.5 mmol) in THF (50 mL) at −75° C. and the mixture was allowed to warm to ambient temperature. After 1 h, the reaction was cooled to −75° C. and 2-(2-bromoethoxy)tetrahydro-2H-pyran (7.15 mL, 47.3 mmol) was added dropwise over 10 min. After 18 h, the mixture was partitioned between EtOAc (100 mL) and H2O (100 mL). The layers were separated and the aqueous layer was further extracted with EtOAc (2×50 mL). The combined organics were dried over Na2SO4, filtered, and concentrated in vacuo. Purification by silica gel chromatography, eluting with a gradient of hexane:EtOAc-100:0 to 80:20, gave the title compound. MS: 71/z=390 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003792B2
Source datasetuspto-grants-2011_08
ORD IDord-182bcd00c12341f7b270023bbc2aac9e
Source noteuspto-grants-2011_08