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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258835Generated: October 25, 2026

5-Bromo-2-chlorobenzaldehyde → (4-benzylspiro[3H-1,4-benzoxazine-2,1-cyclopropane]-6-yl)-(5-bromo-2-chloro-phenyl)methanol

https://huagongshe.com/reaction/1258835

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-2-chlorobenzaldehydeHCID 10608925—
Reactant4-benzyl-6-bromo-spiro[3H-1,4-benzoxazine-2,1-cyclopropane]HCID 58340778—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product(4-benzylspiro[3H-1,4-benzoxazine-2,1-cyclopropane]-6-yl)-(5-bromo-2-chloro-phenyl)methanolHCID 5834078049.4%

Reaction Steps

To a stirred solution of 4-benzyl-6-bromo-spiro[3H-1,4-benzoxazine-2,1′-cyclopropane] (1.12 g, 3.4 mmol) in THF (10 mL) was added 1.6 M solution of n-BuLi in hexanes (2.12 mL, 3.4 mmol) at −78° C. The reaction mixture was stirred for 30 min, and then transferred to a stirred solution of 5-bromo-2-chlorobenzaldehyde (745 mg, 3.4 mmol) in THF (10 mL) at −78° C. After stirring for 1 h, the reaction was quenched by the addition of saturated ammonium chloride solution and extracted with ethyl acetate. The ethyl acetate layer was washed with water, brine, dried over sodium sulphate, and concentrated. The resulting residue was purified by silica gel column chromatography to furnish (4-benzylspiro[3H-1,4-benzoxazine-2,1′-cyclopropane]-6-yl)-(5-bromo-2-chloro-phenyl)methanol (790 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466114B2
Source datasetuspto-grants-2013_06
ORD IDord-63186bcc229244e5af75a26b48b8d956
Source noteuspto-grants-2013_06