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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1631666Generated: October 26, 2026

Gramine → (2,3-dihydro-1H-indol-3-ylmethyl)dimethylamine

https://huagongshe.com/reaction/1631666

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGramineHCID 6890—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventTrifluoroacetic acidHCID 6422—
Product(2,3-dihydro-1H-indol-3-ylmethyl)dimethylamineHCID 1315605865.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

1.1 g of sodium cyanoborohydride is gradually added to a solution of 1 g of gramine in 20 ml of trifluoroacetic acid, under argon, cooled in an ice bath, and stirred for half an hour at 0° C. and then for 2 h at ambient temperature. The reaction medium is plunged into 50 g of ice and alkalinized using 30% sodium hydroxide, and is then extracted with four times 30 ml of ethyl acetate. The organic phase is washed with 20 ml of water, dried over anhydrous magnesium sulphate, filtered, and then concentrated to dryness under reduced pressure. After a silica column purification, eluent: 85/15 v/v CH2Cl2/MeOH, 660 mg of (2,3-dihydro-1H-indol-3-ylmethyl)dimethylamine are obtained in the form of a yellow solid, the characteristics of which are the following:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791255B2
Source datasetuspto-grants-2014_07
ORD IDord-7d4239c7c1bd4c5cb5a96eaa374e3781
Source noteuspto-grants-2014_07