Methanol → 3-(2-Methylpropoxy)azetidine hydrochloride

HRID 2172050Notes

Reaction equation

HRID 2172050 reaction equation
[Cl:1]C(OC(Cl)C)=O.C([N:21]1[CH2:24][CH:23]([O:25][CH2:26][CH:27]([CH3:29])[CH3:28])[CH2:22]1)(C1C=CC=CC=1)C1C=CC=CC=1.CO>ClCCCl>[ClH:1].[CH2:26]([O:25][CH:23]1[CH2:24][NH:21][CH2:22]1)[CH:27]([CH3:29])[CH3:28]

Participants

5

Conditions

Temperature
70 °C

Procedure

1-Chloroethyl chloroformate (83 μL, 0.77 mmol) was added to a solution of 1-benzhydryl-3-isobutoxyazetidine (175 mg, 0.60 mmol) in 1,2-dichloroethane (3 mL) at room temperature. The reaction mixture was then heated up to 70° C. and stirred for 1.5 hours. After cooling down to room temperature, methanol (3 mL) was added and the reaction mixture was heated again to 70° C. and stirred for an additional 1.5 hours. After concentration to dryness, the crude mixture was triturated in pentane (2×5 mL) to give a yellow oil (98 mg, quantitative) which was used in the next step without further purification.

Workup

  1. temperatureAfter cooling down to room temperature
  2. temperaturethe reaction mixture was heated again to 70° C.
  3. stirringstirred for an additional 1.5 hours
  4. concentrationAfter concentration to dryness
  5. customthe crude mixture was triturated in pentane (2×5 mL)
  6. customto give a yellow oil (98 mg, quantitative) which
  7. customwas used in the next step without further purification

Sources & evidence

ORD record
ord-461b56ebb0174d0381bd0be85cac6d5d
Source dataset
uspto-grants-2015_06
Patent number
US09051321B2

Reaction notes

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