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HRID 420880作成日:2026年10月26日

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

https://huagongshe.com/reaction/420880

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物1,5-DibromopentaneHCID 8100—
反応物Delta-ValerolactoneHCID 10953—
反応物MagnesiumHCID 5462224—
反応物3,3-DibromopentaneHCID 13555730—
溶媒TetrahydrofuranHCID 8028—
生成物1-(4'-Hydroxy-n-butyl)-1-cyclohexanolHCID 1562076973.6%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08097728B2
出典データセットuspto-grants-2012_01
ORD IDord-198eff842faa45ba93ef1839348a80c3
出典メモuspto-grants-2012_01