1,3-Dibromopropane → 4-(3-Bromopropoxy)-2,2-dimethyl-1-(1-piperidinyl)indan

HRID 1905755Notes

Reaction equation

HRID 1905755 reaction equation
[OH-].[K+].[CH3:3][C:4]1([CH3:20])[CH2:12][C:11]2[C:6](=[CH:7][CH:8]=[CH:9][C:10]=2[OH:13])[CH:5]1[N:14]1[CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]1.[Br:21][CH2:22][CH2:23][CH2:24]Br>C(Cl)Cl.[Cl-].C([N+](CCCC)(CCCC)CCCC)CCC>[Br:21][CH2:22][CH2:23][CH2:24][O:13][C:10]1[CH:9]=[CH:8][CH:7]=[C:6]2[C:11]=1[CH2:12][C:4]([CH3:20])([CH3:3])[CH:5]2[N:14]1[CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]1

Participants

6

Reactant 3

HCID 80011,3-DibromopropaneHCID 14797Potassium HydroxideHCID 20137132HCID 20137132, compound

Product 1

HCID 201371304-(3-Bromopropoxy)-2,2-dimethyl-1-(1-piperidinyl)indan

Reagents, catalysts & solvents 2

HCID 70681Tetrabutylammonium ChlorideCatalystHCID 6344DichloromethaneSolvent2×

Procedure

Potassium hydroxide (1.44 g) is added to a stirred solution of the 4-hydroxy compound of Step 4. above (5 g) in methylene chloride (44 ml) and stirring is continued under N2 for 30 min. 1,3-Dibromopropane (20.7 ml) and tetrabutyl ammonium chloride (0.63 g) are added and the mixture is stirred at RT for about 70 hours. The reaction mixture is diluted with methylene chloride, washed with H2O, dried, filtered and the filtrate evaporated in vacuo. The residue is chromatographed (silica gel, hexane/ether) affording the purified desired product as an oil.

Workup

  1. washwashed with H2O
  2. customdried
  3. filtrationfiltered
  4. customthe filtrate evaporated in vacuo
  5. customThe residue is chromatographed (silica gel, hexane/ether)
  6. customaffording the
  7. custompurified desired product as an oil

Sources & evidence

ORD record
ord-5ec9cc7bbb4c450db260fb5b569bc21d
Source dataset
uspto-grants-1987_03
Patent number
US04647559

Reaction notes

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