HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 928104Generated: October 31, 2026
HCID 178418573, compound → HCID 178468180, compound
https://huagongshe.com/reaction/928104
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Reactant | HCID 178502729 | HCID 178502729 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178468180 | HCID 178468180 | — |
Reaction Steps
To a solution of benzyl {trans-4-[methoxy(methyl)carbamoyl]cyclohexyl}carbamate (3.43 g, 10.71 mmol) in THF (107 mL) at 0° C. was added methylmagnesium bromide (3.0 M in diethyl ether, 5.35 mL, 16.06 mmol) and the reaction was stirred for one hour at 0° C. An additional portion of methylmagnesium bromide (3.0 M in diethyl ether, 5.35 mL, 16.06 mmol) was then added and the reaction was allowed to warm to room temperature and then stirred for one hour. The reaction was slowly quenched with aqueous saturated ammonium chloride. Water and ethyl acetate were added and the organic layer was separated, dried over magnesium sulfate, filtered and concentrated to afford benzyl (trans-4-acetylcyclohexyl)carbamate that was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09290490B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-e6cd24a2b35c4a7b9689aeae7d4b3503 |
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| Source note | uspto-grants-2016_03 |
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