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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 420880생성일: 2026년 10월 26일

Iodine → 1-(4'-Hydroxy-n-butyl)-1-cyclohexanol

https://huagongshe.com/reaction/420880

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물1,5-DibromopentaneHCID 8100—
반응물Delta-ValerolactoneHCID 10953—
반응물MagnesiumHCID 5462224—
반응물3,3-DibromopentaneHCID 13555730—
용매TetrahydrofuranHCID 8028—
생성물1-(4'-Hydroxy-n-butyl)-1-cyclohexanolHCID 1562076973.6%

반응 단계

A solution of 1,5-dibromopentane (5 gms, 23.15 mmol) in dry THF (10 ml) was added slowly to a suspension of Magnesium turning (2.8 gms, 112 mmole) in dry THF (50 ml) and catalytic amount of iodine under nitrogen atmosphere. After the addition of about 3 ml of dibromopentane solution in THF, Grignard reaction was initiated. The addition was continued maintaining a gentle reflux. The mixture was refluxed for 16 hours to complete the formation of the Grignard reagent. To the reaction mixture was added a solution of a solution of δ-valerolactone (2.13 gms, 21.3 mmol) in dry THF (50 ml). The resulting mixture was refluxed for 6 hours under nitrogen and then quenched by addition of saturated solution of ammonium chloride at 0° C. The product was extracted in ethylacetate. Organic layer was washed with water, brine and dried over anh. Na2SO4. Drying agent was filtered off and the solvent was removed under vacuum to give 2.7 gms of diol (8), which was used without any further purification in the next step.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08097728B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-198eff842faa45ba93ef1839348a80c3
출처 메모uspto-grants-2012_01