HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650342Generated: October 28, 2026
Ammonium Chloride → 3-Benzyloxy-7alpha-(5-hydroxypentyl)-15beta-methyl-estra-1,3,5(10)-trien-17-one
https://huagongshe.com/reaction/650342
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 3-Benzyloxy-7alpha-(5-hydroxypentyl)-estra-1,3,5(10),15-tetra-en-17-one | HCID 57272166 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-Benzyloxy-7alpha-(5-hydroxypentyl)-15beta-methyl-estra-1,3,5(10)-trien-17-one | HCID 69963503 | — |
Reaction Steps
5.35 g of copper(I) iodide is added to an ice-cooled solution of 11.9 ml of a 3-molar methylmagnesium bromide solution in 68 mnl of tetrahydrofuran under a nitrogen stream. Then, a solution of 4.26 g of 3-benzyloxy-7α-(5-hydroxypentyl)-estra-1,3,5(10),15-tetraen-17-one (see Example 6b) in 50 ml of tetrahydrofuran is added in drops and stirred for 30 minutes at a bath temperature of 0° C. Then, the excess reagent is decomposed with saturated ammonium chloride solution, diluted with ethyl acetate, washed with ammonium chloride solution and water, dried on sodium sulfate, concentrated by evaporation in a vacuum and chromatographed on silica gel with hexane/acetone. 3.6 g of 3-benzyloxy-7α-(5-hydroxypentyl)-15β-methyl-estra-1,3,5(10)-trien-17-one is obtained as oil. [α]D22 =+66.4°(c=0.515% in chloroform).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06271403B1 |
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| Source dataset | uspto-grants-2001_08 |
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| ORD ID | ord-7f6ad95d646c4bed8b9def36ca0ce3d0 |
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| Source note | uspto-grants-2001_08 |
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