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HRID 591911생성일: 2026년 10월 26일

Methanol → 3alpha-Hydroxy-7-oxo-5beta-cholan-24-oic acid methyl ester

https://huagongshe.com/reaction/591911

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Sulfuric AcidHCID 1118—
반응물7-Ketolithocholic acidHCID 444262—
생성물3alpha-Hydroxy-7-oxo-5beta-cholan-24-oic acid methyl esterHCID 9931088—

반응 단계

3α-hydroxy-7-keto-5β-cholan-24-oic acid (KLCA; 500.0 g, 1.28 mol) was esterified using methyl alcohol (2500 mL), in the presence of acidic catalysis (sulfuric acid, 1.0 mL) and was heated up to 62° C. to 64° C. for approximately 3 hours, to yield 3α-hydroxy-7-keto-5β-cholan-24-oic acid methyl ester (1). In this reaction, the methyl alcohol acts as the methylating reagent as well as the reaction solvent. For the work-up, the pH-value was adjusted with sodium hydroxide solution (2N) to pH 7.0 to 7.5. The solution was treated with activated carbon (25 g) for approximately 30 minutes and filtered to remove the carbon solids. Alternatively, the solution was not treated with activated carbon. To precipitate the product, water (625 mL) at 10° C. to 15° C. was added over 15 minutes and seeding material was added. The reaction mixture is stirred for 1 hour at 10° C. to 15° C. Another portion of water (1875 mL) was added over about 20 to 25 minutes. The product suspension was stirred for 30 minutes at 10° C. to 15° C. The product was isolated with a centrifuge and washed with a mixture of methanol and water (1:1, 350 mL). The water content of the wet material was quantified by Karl Fischer (KF). The material was dried in a tumble dryer under vacuum at NMT 70° C. The material can also be used in the next step without drying. The yield (calculated on dried product) is 501.4 g (1.24 mol, 96.8%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09238673B2
출처 데이터셋uspto-grants-2016_01
ORD IDord-b4488afaf09840c0807248c785a5fea6
출처 메모uspto-grants-2016_01