HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373997Generated: October 30, 2026
Sulfuric acid magnesium salt (1:1) → F-15063
https://huagongshe.com/reaction/1373997
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric acid magnesium salt (1:1) | HCID 24083 | — |
| Reactant | Potassium borohydride | HCID 4192641 | — |
| Reactant | HCID 12094928 | HCID 12094928 | — |
| Reactant | HCID 16109477 | HCID 16109477 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | F-15063 | HCID 10248159 | 51.5% |
Reaction Steps
1.5 g of magnesium sulfate are added to a solution of 3-cyclopenten-1-ylbenzaldehyde (2a) (0.56 g, 3.26 mmol) and of [2-(2,2-dimethyl-2,3-dihydrobenzofuran-7-yl-oxy)]ethylamine (3a) (0.68 g, 3.26 mmol) in 15 ml of 1,2-dichloroethane and the mixture is heated at 60° C. for 17 hours. The mixture is cooled to room temperature, the solid is filtered and the solvent is evaporated under reduced pressure. The residue is diluted with 15 ml of methanol and then cooled to 0° C. 0.35 g of potassium borohydride (6.52 mmol) is then introduced and the reaction mixture is stirred for 3 hours at 0° C. The mixture is then poured into ice-cold water, extracted with ethyl acetate and washed with a saturated aqueous sodium chloride solution. The combined organic phases are dried over magnesium sulfate, filtered and the solvent is evaporated under reduced pressure. The residue is purified by chromatography on silica gel (methylene chloride/methanol/aqueous ammonia: 98/1.5/0.5). The title product (0.61 g) is isolated in the form of a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07163957B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-b74206b81c02401283790deccbea8468 |
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| Source note | uspto-grants-2007_01 |
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