HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1921691Generated: October 30, 2026
Sodium borohydride → HCID 57577369, compound
https://huagongshe.com/reaction/1921691
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Diethyl acetamido(6-octyl-1-oxo-1,2,3,4-tetrahydronaphthalen-2-yl)propanedioate | HCID 57577370 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 57577369 | HCID 57577369 | 75.6% |
Reaction Steps
To a solution of sodium borohydride (75 mg, 2.00 mmol) in 5 ml of ethanol at room temperature is added 2-acetylamino-2-(6-octyl-1-oxo-1,2,3,4-tetrahydro-naphthalen-2-yl)-malonic acid diethyl ester (compound 5) (1.00 g, 2.1 mmol) in 5 ml of ethanol. The reaction mixture is stirred at room temperature under argon for an additional hour, quenched by the addition of water (20 mL) and methylene chloride (20 mL). The organic layer is removed and the aqueous layer is extracted with methylene chloride (2×20 mL). The combined organic layers were washed with brine (2×20 mL) and dried over magnesium sulfate and concentrated under vacuum. The residue is purified by column chromatography (silica gel, 20% ethyl acetate in hexanes) to provide 755 mg of compound A (75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08173710B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-32b0801000f94920870d7ca21932cfb3 |
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| Source note | uspto-grants-2012_05 |
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