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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2395119Generated: November 3, 2026

Diethyl Ether → HCID 18972543, compound

https://huagongshe.com/reaction/2395119

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 18972633HCID 18972633—
ReactantButyllithiumHCID 178418339—
ProductHCID 18972543HCID 1897254395.75%

Reaction Steps

8.6 ml of n-butyllithium solution (1.6M in hexane) were added dropwise at -78° to a solution of 3.3 g (11.49 mmol) of 3,7-dimethoxy-10-methyl-10H-dibenzo[b,e][1,4]oxazine-4-methanol in 33 ml of absolute tetrahydrofuran, whereby a white precipitate formed. The reaction mixture was brought to 0°, stirred for 30 minutes, treated at 0° with 1.96 ml (1.5 eq.) of 2-(methoxyethoxy)methyl chloride, stirred at room temperature for 1 hour and then poured into ice, saturated ammonium chloride solution and diethyl ether. The organic phase was dried over magnesium sulphate and evaporated. The residue was chromatographed on silica gel with a mixture of ethyl acetate/hexane (1:2), whereupon, after drying in a high vacuum, 4.13 g (95.75%) of 3,7-dimethoxy-4-[[(2-methoxyethoxy)methoxy]methyl]-10-methyl-10H-dibenzo[b,e][1,4]oxazine were obtained as a colourless oil. MS: 375 (M+, 100), 360(11), 270(14), 256(21), 226(14).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05811389
Source datasetuspto-grants-1998_09
ORD IDord-690bf560023d49828c486785f116cede
Source noteuspto-grants-1998_09