Hydroxyprogesterone caproate synthesis
- Product Name:Hydroxyprogesterone caproate
- CAS Number:630-56-8
- Molecular formula:C27H40O4
- Molecular Weight:428.6
68-96-2
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$35.00/25mg
142-62-1
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630-56-8
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$50.00/5 g
Yield:630-56-8 19.8 g
Reaction Conditions:
Stage #1:17-hydroxyprogesterone;hexanoic acid with pyridine;toluene-4-sulfonic acid in toluene at 110 - 120; for 3 h;
Stage #2: with hydrogenchloride in ethanol;water for 2 h;Reflux;Reagent/catalyst;Solvent;
Steps:
1
17α- hydroxy progesterone 20g, n-hexanoic acid 40ml, pyridine 16ml, p-toluenesulfonic acid 1.6g, toluene300ml, into 500ml three-necked flask, the reaction temperature was raised to between 110 ~ 120°C 3 hours. sampling The reaction was monitored by TLC. The reaction is as follows 17α- hydroxyprogesterone concentration treatment made after completion of the reaction,concentration treatment method for a concentrated under reduced pressureToluene, pyridine and n-hexanoic acid. After concentration in a three-neck flask was added the end of 100ml of ethanol, in 3 ml of concentrated hydrochloric acid, heated under reflux, alcohol solution for 2 hours. Sampling the reaction was monitored by TLC, complete hydrolysis of the diester into progesterone caproate after the reaction was stopped. The reaction is as follows: n-caproic acid was cooled to below 5 ° C, filtration, drying in progesterone caproate crude 24g, crude yield 120%. Progesterone caproate crude product was purified with ethanol to give progesterone caproate boutique 19. 8g, progesterone caproate Collectibles The yield progesterone caproate crude 82.5%, the total yield of 99.0%.
References:
Jiangsu Grand Xinyi Pharmaceutical Co.,Ltd.;KONG, LEI CN104017041, 2016, B Location in patent:Paragraph 0013-0015; 0017-0019
94201-44-2
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630-56-8
341 suppliers
$50.00/5 g
2051-49-2
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$16.00/25mL
630-56-8
341 suppliers
$50.00/5 g
20867-15-6
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630-56-8
341 suppliers
$50.00/5 g
2051-49-2
183 suppliers
$16.00/25mL
68-96-2
435 suppliers
$35.00/25mg
630-56-8
341 suppliers
$50.00/5 g