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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 501811생성일: 2026년 10월 26일

Hexamethylenetetramine → Methyl 4-formyl-3-methoxybenzoate

https://huagongshe.com/reaction/501811

반응식

참여 물질

역할이름HCID투입량
반응물HexamethylenetetramineHCID 4101—
반응물AzobisisobutyronitrileHCID 6547—
반응물N-bromobutanimideHCID 67184—
반응물Benzoic acid, 3-methoxy-4-methyl-, methyl esterHCID 591123—
용매Acetic AcidHCID 176—
용매BenzeneHCID 241—
용매WaterHCID 962—
생성물Methyl 4-formyl-3-methoxybenzoateHCID 1063165064.6%

반응 단계

2.50 g of methyl 3-methoxy-4-methylbenzoate was dissolved in 25 mL of benzene, to which 2.72 g of N-bromosuccinimide and 0.23 g of 2,2′-azobisisobutyronitrile were successively added at room temperature, and this solution was stirred for one hour while heating it under reflux. After 3.90 g of hexamethylenetetramine dissolved in 7.8 mL of acetic acid and 7.8 mL of water was added dropwise to the reaction mixture, benzene was distilled out therefrom, and then the mixture was stirred for one hour while heating it under reflux. The reaction mixture, which was cooled to room temperature, was added to a mixture of chloroform and water and then adjusted to pH 7 with a 20% aqueous solution of sodium hydroxide, and the organic phase was separated therefrom. After the resultant organic phase was successively washed with water, a saturated aqueous solution of sodium hydrogen carbonate, and a saturated sodium chloride solution, the washed phase was dried over anhydrous magnesium sulfate, and the solvent was distilled out under reduced pressure. The resultant residue was purified by silica gel column chromatography [eluent; hexane:ethyl acetate=3:1] to yield 1.74 g of methyl 4-formyl-3-methoxybenzoate as white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07772285B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-a3ef6e1c4ac3432e90d3632acd088c9b
출처 메모uspto-grants-2010_08