HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1695842Generated: 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/1695842
Participants
| Role | Name | HCID | Charge |
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| Reactant | 5-Bromo-2-chlorobenzaldehyde | HCID 10608925 | — |
| Reactant | 4-benzyl-6-bromo-spiro[3H-1,4-benzoxazine-2,1-cyclopropane] | HCID 58340778 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (4-benzylspiro[3H-1,4-benzoxazine-2,1-cyclopropane]-6-yl)-(5-bromo-2-chloro-phenyl)methanol | HCID 58340780 | 49.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08163704B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-34091c2304cc42dd864e9bc4df8f9fec |
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| Source note | uspto-grants-2012_04 |
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