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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337636Generated: November 4, 2026

Methane → Tert-butyl cyclopropyl(3-(3-methoxypropyl)-5-methylbenzyl)carbamate

https://huagongshe.com/reaction/337636

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
Reactanttert-Butyl cyclopropyl{3-formyl-5-[(1E)-3-methoxy-1-propen-1-yl]benzyl}carbamateHCID 86651678—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl cyclopropyl(3-(3-methoxypropyl)-5-methylbenzyl)carbamateHCID 86651679—

Reaction Steps

tert-Butyl cyclopropyl{3-formyl-5-[(1E)-3-methoxy-1-propen-1-yl]benzyl}carbamate (1 eq.) from the previous step and 10% w/w palladium over charcoal (0.1 eq.) were suspended in EtOAc (0.1 M). The vessel was then evacuated and purged with H2. Under a balloon-filled H2 atmosphere, the reaction suspension was stirred at RT for 3 h. The reaction suspension was then quenched with dichloromethane and filtered through a bed of celite. Concentration of the filtrate in vacuo to afford the title compound as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889714B2
Source datasetuspto-grants-2014_11
ORD IDord-787d61e977d94025a2fff4ba35496566
Source noteuspto-grants-2014_11