Water → HCID 54447967, compound

HRID 264536Notes

Reaction equation

HRID 264536 reaction equation
O=CC[CH:4]1[CH2:13][C:12](=O)[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[O:5]1.O.[NH2:16][CH2:17][C@@H:18]([OH:20])[CH3:19].[C:21]1(C)C=CC=C[CH:22]=1>C1(C)C=CC(S(O)(=O)=O)=CC=1>[N:16]1([CH2:17][C@@H:18]([OH:20])[CH3:19])[CH:22]=[CH:21][C:13]2[CH2:4][O:5][C:6]3[CH:7]=[CH:8][CH:9]=[CH:10][C:11]=3[C:12]1=2

Participants

6

Reactant 4

HCID 962WaterHCID 1140Toluene2×HCID 7311736(S)-(+)-1-Aminopropan-2-olHCID 13926372HCID 13926372, compound

Product 1

HCID 54447967HCID 54447967, compoundYield 76%

Reagents, catalysts & solvents 1

HCID 6101p-Toluenesulfonic acidCatalyst

Procedure

A solution of 1.9 g of (RS)-2-(2-oxoethyl)-4-chromanone and 80 mg of p-toluenesulfonic acid in 70 ml of anhydrous toluene was heated on a water separator. A solution of 3.0 g of (S)-1-amino-2-propanol in 20 ml of anhydrous toluene was added dropwise to the boiling solution over a period of 5 minutes. Subsequently, the mixture was boiled for an additional 35 minutes, during which the solvent was reduced to a volume of 20 ml. The cooled reaction mixture was purified by column chromatography on silica gel (ethyl acetate/toluene 2:3). 1.73 g (76%) of (S)-1-(1,4-dihydro-[1]benzopyrano[4,3-b]pyrrol-1-yl)-propan-2-ol were obtained as a yellow oil.

Workup

  1. customThe cooled reaction mixture
  2. customwas purified by column chromatography on silica gel (ethyl acetate/toluene 2:3)

Sources & evidence

ORD record
ord-e0908e071bcd4ba29d73c688647bea16
Source dataset
uspto-grants-1997_07
Patent number
US05646173

Reaction notes

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