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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1012933Generated: October 25, 2026

rac-tert-butyl N-[(1r,4r)-4-formylcyclohexyl]carbamate → HCID 178489240, compound

https://huagongshe.com/reaction/1012933

Reaction equation

Participants

RoleNameHCIDCharge
Reactantrac-tert-butyl N-[(1r,4r)-4-formylcyclohexyl]carbamateHCID 11020615—
Reactant4-Methoxy-1,3-benzothiazoleHCID 12631858—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178489240HCID 17848924053%

Reaction Steps

To a solution of 4-methoxy-benzothiazole (1.65 g, 10 mmol) in THF (50 ml) was added dropwise n-BuLi (2.5M in hexanes, 4 ml) so that the temperature did not exceed −70° C. The brown solution was stirred at this temperature for 15 min before dropwise addition of a solution of (4-formyl-cyclohexyl)-carbamic acid tert-butyl ester (1.14 g, 5 mmol) in THF (10 ml). The temperature was kept below −70° C. The brown solution was then gradually allowed to reach RT (over 3 h). The reaction mixture was quenched with saturated NH4Cl solution and extracted with EtOAc. The organic layer was washed with brine and dried over MgSO4 and concentrated under reduced pressure. The product was crystallised from ether to give 1.04 g (53%) of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981886B2
Source datasetuspto-grants-2011_07
ORD IDord-728534994fab4e25b1ea419fa9a3127e
Source noteuspto-grants-2011_07