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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 226365Generated: October 30, 2026

4-Methylbenzyl chloride → HCID 53256309, compound

https://huagongshe.com/reaction/226365

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methylbenzyl chlorideHCID 7722—
ReactantDiisopropylethylamineHCID 81531—
Reactant(3R)-(+)-3-(tert-Butoxycarbonylamino)pyrrolidineHCID 1514397—
SolventDimethylformamideHCID 6228—
ProductHCID 53256309HCID 5325630975.2%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a mixture of tert-butyl (3R)-3-pyrrolidinylcarbamate (4.0 g) and 1-(chloromethyl)-4-methylbenzene (3.17 g) in DMF(40 mL) was added N-ethyl-N-isopropyl-2-propanamine (5.55 g) at ambient temperature and the resulting mixture was heated at 70° C. for four hours. The mixture was allowed to cool to ambient temperature and extracted with ethyl acetate (100 mL). The organic phase was washed with water (50 mL) and brine (50 mL). The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was purified by a flash chromatography eluting with gradient solvent system (ethyl acetate-hexane from 1:4 v/v to 1:1 v/v) to give tert-butyl [(3R)-1-(4-methylbenzyl)-3-pyrrolidinyl]carbamate (4.69 g) as a pale yellow syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557127B2
Source datasetuspto-grants-2009_07
ORD IDord-5945a60561544ab6be9609273fa7c69e
Source noteuspto-grants-2009_07