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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2356966Generated: November 1, 2026

tert-Butyl 4-(bromomethyl)piperidine-1-carboxylate → HCID 21959486, compound

https://huagongshe.com/reaction/2356966

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-(bromomethyl)piperidine-1-carboxylateHCID 15512811—
Reactant3,3-Dimethyl-6-nitroindolineHCID 21959466—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethylformamideHCID 6228—
ProductHCID 21959486HCID 21959486—

Reaction Conditions

Temperature100 °C

Reaction Steps

A process vial with a suspension of 1 g 3,3-dimethyl-6-nitro-2,3-dihydro-1H-indole, 1.59 g 4-bromomethyl-piperidine-1-carboxylic acid tert-butyl ester and 1.17 g potassium tert-butoxide in 10 ml N,N-dimethylformamide was sealed with a teflon septum and placed in the microwave cavity. The reaction mixture was stirred for 15 minutes at 100° C. by microwave-assisted heating (Emrys Optimizer, Personal Chemistry). After removal of the solvent under reduced pressure the residue was purified by flash chromatography on silica gel with a n-heptane/ethylacetate gradient. The fractions containing the product were combined and evaporated to yield a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759379B2
Source datasetuspto-grants-2010_07
ORD IDord-03e4597ed6ec44969cfa1d297ebe0403
Source noteuspto-grants-2010_07