Triethylamine → Phenylmethyl 1,4-dioxa-8-azaspiro[4.5]decane-8-carboxylate

HRID 1585563Notes

Reaction equation

HRID 1585563 reaction equation
[O:1]1[C:5]2([CH2:10][CH2:9][NH:8][CH2:7][CH2:6]2)[O:4][CH2:3][CH2:2]1.C(N(CC)CC)C.[CH2:18]([O:25][C:26](Cl)=[O:27])[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1>ClCCl>[CH2:18]([O:25][C:26]([N:8]1[CH2:9][CH2:10][C:5]2([O:4][CH2:3][CH2:2][O:1]2)[CH2:6][CH2:7]1)=[O:27])[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1

Participants

5

Reactant 3

HCID 8471TriethylamineHCID 10387Benzyl chloroformateHCID 674351,4-Dioxa-8-azaspiro(4.5)decane

Product 1

HCID 15165038Phenylmethyl 1,4-dioxa-8-azaspiro[4.5]decane-8-carboxylate

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

To a well-stirred and ice-cooled solution of 1,4-dioxa-8-azaspiro[4,5]decane (34.9 mmol, 5 g) in dichloromethane (200 mL) under an argon atmosphere, was added triethylamine (52.4 mmol, 7.3 mL) and then benzyloxycarbonyl chloride (42 mmol, 5.93 mL) dropwise. The suspension was stirred at room temperature for 24 hours and the precipitated solid was filtered. The organic solution was evaporated under vacuum to give an oily residue which was chromatographed on silica gel eluting with ethyl ether and petroleum ether mixture to afford 8-benzyloxycarbonyl 1,4-dioxa-8-azaspiro [4,5]decane in quantitative yield.

Workup

  1. stirringThe suspension was stirred at room temperature for 24 hours
  2. filtrationthe precipitated solid was filtered
  3. customThe organic solution was evaporated under vacuum
  4. customto give an oily residue which
  5. customwas chromatographed on silica gel eluting with ethyl ether and petroleum ether mixture

Sources & evidence

ORD record
ord-ed817f2e90d34072aba26084f83d03cd
Source dataset
uspto-grants-1999_08
Patent number
US05939432

Reaction notes

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