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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 27659생성일: 2026년 10월 25일

Benzene → Methyl Tri(3-pentyl)tin

https://huagongshe.com/reaction/27659

반응식

참여 물질

역할이름HCID투입량
반응물BenzeneHCID 241—
반응물Sulfuric AcidHCID 1118—
반응물3-BromopentaneHCID 15738—
반응물TrichloromethylstannaneHCID 101940—
반응물MagnesiumHCID 5462224—
반응물HCID 178456026HCID 178456026—
촉매1,2-DibromoethaneHCID 7839—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물Methyl Tri(3-pentyl)tinHCID 8673720785%

반응 단계

To 16 g. (0.66 g. atom) of magnesium turnings maintained at a temperature of 25° C. under a nitrogen atmosphere was added a 25 cc. portion of a solution containing 99.7 g. (0.66 mole) of 3-bromopentane dissolved in 300 cc. of anhydrous tetrahydrofuran. The reaction was initiated using a few drops of ethylene dibromide. The remaining portion of the 3-bromopentane solution was gradually added during a period of one hour while the reaction mixture was heated to the boiling point. Heating was continued for an additional hour. The reaction mixture was then allowed to cool to ambient temperature, at which time all of the magnesium appeared to have reacted. The resultant solution contained 0.6 mole of 3-pentyl magnesium bromide, and was added dropwise to a stirred solution of methyltin trichloride (49 g., 0.2 mole) dissolved in 50 cc. of dry benzene. The addition required 0.5 hour and was conducted under a nitrogen atmosphere. During the addition the temperature of the reaction mixture rose to 71° C. Following completion of the addition the reaction mixture was heated to the boiling point for one hour, then allowed to cool to ambient temperature. To the resultant mixture was added a solution containing 250 cc. water and 15 cc. concentrated sulfuric acid over a five minute period. The aqueous phase was separated and the residual was removed by combining the organic phase with a portion of anhydrous magnesium sulfate, which was subsequently removed by filtration. The solvent was evaporated under reduced pressure to yield 58.8 g. (85% yield) of a yellow liquid exhibiting a refractive index (nD25) of 1.4954. This product was extracted twice with methanol and distilled under reduced pressure. The fraction boiling from 81° to 87° C. under a pressure of 0.15 mm. was isolated and exhibited a refractive index (nD22) of 1.4920. Analysis by vapor phase chromatography indicated that the product was 95.7% pure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04222950
출처 데이터셋uspto-grants-1980_09
ORD IDord-19bbd6f4c90a44ebbae1fb166d5ad7ff
출처 메모uspto-grants-1980_09