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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1724014Generated: October 30, 2026

Benzyl Bromide → 1-benzylindoline

https://huagongshe.com/reaction/1724014

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantIndolineHCID 10328—
ReactantPotassium CarbonateHCID 11430—
ReactantAmmonium ChlorideHCID 25517—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product1-benzylindolineHCID 1080509669.5%

Reaction Steps

A solution of 5 g (41.96 mmol) of indoline in DMF was treated with 5.8 g (41.96 mmol) of K2CO3 and then at 0° C. dropwise, under intense stirring, with 5.5 mL (46.2 mmol) of benzylbromide. The mixture was stirred at RT for 10 hrs and then for 2 hrs at 60° C. The resulting thick pulp was distributed between a saturated aqueous solution of NH4Cl and Et2O. Drying of the combined organic phases over Na2SO4 and evaporation of the solvent yielded 6.1 g (69%) of N-benzylindoline MS: 210 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07485652B2
Source datasetuspto-grants-2009_02
ORD IDord-b0de48b42cb846af9b29dfbb69570dcc
Source noteuspto-grants-2009_02