Triethylamine → HCID 57450911, compound

HRID 1641823Notes

Reaction equation

HRID 1641823 reaction equation
[CH3:1][O:2][C:3]([CH:5]1[CH2:10][CH2:9][CH:8](C(O)=O)[CH2:7][CH2:6]1)=[O:4].C([N:16]([CH2:19]C)CC)C.ClC(OCC)=[O:23]>C(Cl)(Cl)Cl>[CH3:1][O:2][C:3]([C:5]1([C:19](=[O:23])[NH2:16])[CH2:6][CH2:7][CH2:8][CH2:9][CH2:10]1)=[O:4]

Participants

5

Procedure

To a mixture cyclohexane-1,4-dicarboxylic acid monomethyl ester (3 g, 16.1 mmol) and triethylamine (2.24 mL, 16.1 mmol) in chloroform cooled in an icebath was dripped in of ethyl chloroformate (1.54 g, 16.1 mmol) followed by bubbling of ammonia gas for 15 min. The reaction was stirred for 1 hr, filtered, the precipitate washed with chloroform, the filtrate diluted with dichloromethane (500 mL) and washed with aqueous sodium bicarbonate (saturated, 500 mL) and brine (250 mL), dried over sodium sulfate, and concentrated to give carbamoyl-cyclohexanecarboxylic acid methyl ester (2.1 g, 72%) as a white solid. LCMS calcd for C9H15NO3 (m/e) 185, obsd 186 (M+H).

Workup

  1. customby bubbling of ammonia gas for 15 min
  2. filtrationfiltered
  3. washthe precipitate washed with chloroform
  4. additionthe filtrate diluted with dichloromethane (500 mL)
  5. washwashed with aqueous sodium bicarbonate (saturated, 500 mL) and brine (250 mL)
  6. dry with materialdried over sodium sulfate
  7. concentrationconcentrated

Sources & evidence

ORD record
ord-09febfbc27784d1d8ab82eda5d340cd5
Source dataset
uspto-grants-2012_02
Patent number
US08115011B2

Reaction notes

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