Formaldehyde → HCID 22758150, compound

HRID 442057Notes

Reaction equation

HRID 442057 reaction equation
[NH:1]1[CH2:6][CH2:5][CH2:4][CH2:3][CH:2]1[CH2:7][CH2:8][CH:9]1[C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[CH2:11][CH2:10]1.[CH2:18]=O>C(O)=O>[CH3:18][N:1]1[CH2:6][CH2:5][CH2:4][CH2:3][CH:2]1[CH2:7][CH2:8][CH:9]1[C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[CH2:11][CH2:10]1

Participants

4

Reactant 2

HCID 712FormaldehydeHCID 227581542-[2-(2,3-Dihydro-1H-inden-1-yl)ethyl]piperidine

Product 1

HCID 22758150HCID 22758150, compound

Reagents, catalysts & solvents 1

HCID 284Formic AcidSolvent

Procedure

45 g. of 1-[2-(2-piperidyl)-ethyl]indane prepared as described above is mixed with 100 ml. of 37% formalin and 200 ml. of 98% formic acid is added while swirling and the solution is then heated overnight on a steam bath. The reaction mixture is worked up by concentrating in vacuo, dissolving in water, filtering, basification and extraction with ether. The ether extracts are dried over potassium hydroxide and after removal of the ether, the product is distilled collecting 42.6 g. (88%), N-methyl-1-[2-(2-piperidyl)ethyl]indane, boiling point 128°-130° C/0.2 mm.

Workup

  1. additionabove is mixed with 100 ml
  2. temperaturethe solution is then heated overnight on a steam bath
  3. concentrationby concentrating in vacuo
  4. dissolutiondissolving in water
  5. filtrationfiltering
  6. extractionbasification and extraction with ether
  7. dry with materialThe ether extracts are dried over potassium hydroxide
  8. customafter removal of the ether
  9. distillationthe product is distilled
  10. customcollecting 42.6 g

Sources & evidence

ORD record
ord-5d4211b88f494e7d969fbeb429722ec2
Source dataset
uspto-grants-1977_08
Patent number
US04044040

Reaction notes

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