HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2045129Generated: October 30, 2026
tert-Butyl [(4-oxocyclohexyl)methyl]carbamate → HCID 86647903, compound
https://huagongshe.com/reaction/2045129
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl [(4-oxocyclohexyl)methyl]carbamate | HCID 40424027 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86647903 | HCID 86647903 | — |
Reaction Steps
A solution of tert-butyl (4-oxocyclohexyl)methylcarbamate (1.00 g) was dissolved in tetrahydrofuran (20 mL) and cooled to −78° C. Methylmagnesium bromide (4.40 mL) was added dropwise. The reaction was stirred for 2 hours at −78° C. then allowed to warm to 0° C. and stirred for 30 minutes. The resulting suspension was quenched with water (10 mL), diluted with ether (50 mL) and washed with ammonium chloride (25 mL) and brine (25 mL), dried over magnesium sulfate, filtered, and concentrated. Silica gel chromatography (Reveleris 80 g) eluting using a gradient of 5% to 50% ethyl acetate/dichloromethane over 30 minutes (flow=60 ml/min) gave the title compound as a ˜2:1 mixture of cis and trans isomers.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08586754B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-c690c21ff54e4a46991ab0c462e0ecfa |
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| Source note | uspto-grants-2013_11 |
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