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HRID 610635作成日:2026年10月27日

Acetic Acid → 1,1-Dimethylethyl 6-cyano-3,5-dihydroxyhexanoate

https://huagongshe.com/reaction/610635

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物DiethylmethoxyboraneHCID 522516—
反応物Sodium borohydrideHCID 4311764—
反応物tert-Butyl (R)-6-Cyano-5-hydroxy-3-oxohexanoateHCID 9794547—
溶媒MethanolHCID 887—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物1,1-Dimethylethyl 6-cyano-3,5-dihydroxyhexanoateHCID 22282997—

反応条件

温度-85 °C

反応手順

Crude (5R)-1,1-dimethylethyl 6-cyano-5-hydroxy-3-oxo-hexanoate (Example 4), approximately 52 mol, was dissolved in 90 L of tetrahydrofuran and 19 L of methanol under a nitrogen atmosphere. This solution was cooled to -85° C. and 24 L of a 50% solution of methoxy-diethylborane in tetrahydrofuran was added. The reaction was cooled to -97° C. and 3.6 kg (126 mol) of sodium borohydride was added in 0.2 kg portions over 3 hours. The reaction was maintained between -93° C. and -85° C. for 5 hours and allowed to warm to room temperature and stand for 10 hours under a nitrogen atmosphere. The reaction was quenched by the addition of 7.5 L (118.5 mol) acetic acid and concentrated by vacuum distillation to an oil. The residue was dissolved with 40 L of methanol, concentrated by vacuum distillation, redissolved with 44 L of methanol, and reconcentrated by vacuum distillation to give a brown oil. This oil was taken up in 90 L of ethyl acetate and washed with 30 L of deionized water. The ethyl acetate solution was concentrated by vacuum distillation to give the title compound, [R-(R*,R*)]-1,1-dimethylethyl 6-cyano-3,5-dihydroxyhexanoate, which was used without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05998633
出典データセットuspto-grants-1999_12
ORD IDord-523fde3fbd5543f9b3e40a6680160a96
出典メモuspto-grants-1999_12