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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254280Generated: October 31, 2026

Sodium hydride → HCID 67024819, compound

https://huagongshe.com/reaction/254280

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant1-Bromomethyl-2,6-dichlorobenzeneHCID 30159—
ReactantHCID 16738222HCID 16738222—
ReactantHCID 86638599HCID 86638599—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 67024819HCID 67024819—

Reaction Steps

(1R,2R)/(1S,2S)-2-[1,4-Dioxa-7-azaspiro[4.4]non-7-yl]-1-[(2,6-dichlorophenyl)methoxy]cyclohexane: To a suspension of sodium hydride, 80% oil dispersion (222 mg, 7.25 mmol) in ethyleneglycol dimethyl ether (20 mL) was added a solution of (1R,2R)/(1S,2S)-2-(1,4-dioxa-7-azaspiro[4.4]non-7-yl)cyclohexanol (1.5 g, 6.60 mmol, step (v) of Example 15) in ethylene glycol dimethyl ether (10 mL). The resulting mixture was stirred at room temperature for 2 hours and then a solution of 2,6-dichlorobenzyl bromide (1.9 g, 7.9 mmol) in ethylene glycol dimethyl ether (10 mL) was added. The reaction mixture was refluxed for 16 hours under argon atmosphere, the solvent was evaporated in vacuo and the residue was taken up with water (70 mL). The aqueous solution was acidified to pH 0.5 with 6M HCl aqueous solution and then extracted with diethyl ether (2×40 mL). Basification of the aqueous solution to pH 4.5-5.5, followed by extraction with diethyl ether (4×40 mL), drying of the combined organic extracts over sodium sulfate and evaporation of the solvent in vacuo provided the intermediate title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07875611B2
Source datasetuspto-grants-2011_01
ORD IDord-2eb99ebf396a402d970f797aa3580965
Source noteuspto-grants-2011_01