HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25577Generated: October 26, 2026
Potassium bisulfate → HCID 178486044, compound
https://huagongshe.com/reaction/25577
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium bisulfate | HCID 516920 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 178502727 | HCID 178502727 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178486044 | HCID 178486044 | — |
Reaction Steps
A solution of 2.09 g (55 mmol) LAH in 250 ml THF was cooled (−50° C.) and treated during 25 min with a solution of 15.02 g (50 mmol) of trans-[4-(Methoxy-methyl-carbamoyl)-cyclohexyl]-methyl-carbamic acid tert-butyl ester in 250 ml THF. The reaction was warmed up to +15° C. for 3.5 h, cooled (−78° C.) and hydrolyzed with a suspension of 15 g MgSO4.7H2O, 15 g silicagel in 50 ml aqueous 10% KHSO4. The cooling bath was removed, THF was added, the mixture was stirred for 30 min and filtered. After evaporation, the residue was dissolved in CH2Cl2, dried over Na2SO4 and evaporated to yield 12.83 (quantitative) trans-(4-Formyl-cyclohexyl)-methyl-carbamic acid tert-butyl ester, MS: 241 (M).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06858651B2 |
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| Source dataset | uspto-grants-2005_02 |
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| ORD ID | ord-6022171bfbfc41a88f67c0c30a82e5ba |
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| Source note | uspto-grants-2005_02 |
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