HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743795Generated: October 31, 2026
Potassium bisulfate → HCID 178484048, compound
https://huagongshe.com/reaction/1743795
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium bisulfate | HCID 516920 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 178502718 | HCID 178502718 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178484048 | HCID 178484048 | — |
Reaction Steps
A solution of 12.25 g (313.11 mmol) LAH in 1.3 l THF was cooled (−50° C.) and treated during 30 min with a solution of 89.5 g (284.64 mmol) of trans-[4-(Methoxy-methyl-carbamoyl)-cyclohexylmethyl]-methyl-carbamic acid tert-butyl ester in 1.3 l THF. After 20 min at this temperature, the reaction was warmed up to 0° C., cooled (−78° C.) and hydrolyzed with a suspension of 90 g MgSO4.7H2O, 90 g silicagel in 292 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 90.4 (quantitative) of trans-(4-Formyl-cyclohexylmethyl)-methyl-carbamic acid tert-butyl ester, MS: 255 (M).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07012077B2 |
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| Source dataset | uspto-grants-2006_03 |
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| ORD ID | ord-ecde24ac7aec4859a1cc8f1159b93779 |
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| Source note | uspto-grants-2006_03 |
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