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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 326596Generated: October 25, 2026

2-Methoxypropene → 6-bromo-2,2-dimethyl-4-(1,3-dithian-2-yl)-2H-1,3-benzoxazine

https://huagongshe.com/reaction/326596

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethoxypropeneHCID 8300—
Reactant1,3-DithianeHCID 10451—
Reactant5-Bromo-2-hydroxybenzonitrileHCID 2757014—
Reactant6-bromo-2,2-dimethyl-4-(1,3-dithian-2-yl)-2H-1,3-benzoxazineHCID 19735097—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product6-bromo-2,2-dimethyl-4-(1,3-dithian-2-yl)-2H-1,3-benzoxazineHCID 19735097—
Product5-Bromo-2-(2-methoxy-2-methylethoxy)benzonitrileHCID 19735126—

Reaction Steps

A solution (13.8 ml) of 1.6M n-butyllithium in hexane was added dropwise to a solution of 1,3-dithian (1.5 g) in anhydrous tetrahydrofuran (35 ml) at -78° C. under an argon atmosphere over 10 minutes. After stirring for 30 minutes, a solution of 5-bromo-2-(2-methoxy-2-methylethoxy)benzonitrile, which was prepared from 4-bromo-2-cyanophenol (m.p. 148°-150° C., 2.48 g) and 2-methoxypropene (1.1 g) according to the same manner as described in Example 29, in anhydrous tetrahydrofuran (5 ml) was added to the mixture. The mixture was treated in the same manner as that in Example 29 to obtain 6-bromo-2,2-dimethyl-4-(1,3-dithian-2-yl)-2H-1,3-benzoxazine (0.90 g) (Compound 105).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05270308
Source datasetuspto-grants-1993_12
ORD IDord-30d90ac680874be6916d41865b13c04c
Source noteuspto-grants-1993_12