Ammonia → 1,4-Dioxaspiro[4.5]decane-8-carboxamide

HRID 1802535Notes

Reaction equation

HRID 1802535 reaction equation
[O:1]1[C:5]2([CH2:10][CH2:9][CH:8]([C:11]([OH:13])=O)[CH2:7][CH2:6]2)[O:4][CH2:3][CH2:2]1.C([N:16](CC)CC)C.ClC(OCCC)=O.N>O1CCCC1>[O:1]1[C:5]2([CH2:10][CH2:9][CH:8]([C:11]([NH2:16])=[O:13])[CH2:7][CH2:6]2)[O:4][CH2:3][CH2:2]1

Participants

6

Procedure

To a solution of 1,4-dioxaspiro[4.5]decane-8-carboxylic acid (823 mg, 4.42 mmol) in tetrahydrofuran (22 mL), triethylamine (5.87 mL, 42.1 mmol) and n-propyl chloroformate were added at 0° C., and the obtained solution was stirred at the same temperature for 1 hour. After adding dropwise, the obtained solution was stirred at room temperature for 30 minutes. To the reaction solution, 28% aqueous ammonia (1.5 mL) was added, and the obtained solution was stirred at room temperature for 1 hour. The organic layer was separated from the reaction solution, dried over sodium sulfate and concentrated under reduced pressure. The residue was purified by flash chromatography (silica gel, n-hexane/ethyl acetate) to obtain the captioned compound (694 mg, 3.75 mmol, 85%) as a colorless amorphous product.

Workup

  1. additionAfter adding dropwise
  2. stirringthe obtained solution was stirred at room temperature for 30 minutes
  3. stirringthe obtained solution was stirred at room temperature for 1 hour
  4. customThe organic layer was separated from the reaction solution
  5. dry with materialdried over sodium sulfate
  6. concentrationconcentrated under reduced pressure
  7. customThe residue was purified by flash chromatography (silica gel, n-hexane/ethyl acetate)

Sources & evidence

ORD record
ord-31df7071ad4d43008c2359dfd172ffe9
Source dataset
uspto-grants-2013_01
Patent number
US08349874B2

Reaction notes

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