Sodium Carbonate → HCID 390821, compound

HRID 534011Notes

Reaction equation

HRID 534011 reaction equation
Cl.[OH:2][NH2:3].C(=O)([O-])[O-].[Na+].[Na+].[O:10]1[C:14]2([CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]2)[O:13][CH2:12][C@@H:11]1[CH:20]=O>O.C1COCC1>[O:10]1[C:14]2([CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]2)[O:13][CH2:12][C@@H:11]1[CH:20]=[N:3][OH:2]

Participants

6

Procedure

In 1000 mL of DI water was added hydroxyl amine hydrochloride (51.0 g, 734 mmol) and the reaction was stirred for 5 minutes. Sodium carbonate (38.1 g, 360 mmol) was added in 3 large portions and the reaction was stirred for 15 minutes. THF (700 mL) was added to the reaction and (R)-1,4-dioxaspiro[4.5]decane-2-carbaldehyde (125 g, 734 mmol) was added in 1 portion in 800 mL of THF. The reaction was stirred for 4 hours and poured into a 4 L separatory funnel and the layers separated. The aqueous layer was extracted twice with MTBE (about 3000 mL total). The combined organic layers were washed with water (700 mL) and brine 300 mL), dried over MgSO4 and concentrated in vacuo to afford (S)-1,4-dioxaspiro[4.5]decane-2-carbaldehyde oxime (135 g, 99%) as a clear viscous oil.

Workup

  1. stirringthe reaction was stirred for 15 minutes
  2. stirringThe reaction was stirred for 4 hours
  3. additionpoured into a 4 L separatory funnel
  4. customthe layers separated
  5. extractionThe aqueous layer was extracted twice with MTBE (about 3000 mL total)
  6. washThe combined organic layers were washed with water (700 mL) and brine 300 mL),
  7. dry with materialdried over MgSO4
  8. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-0841c76418144903a1ef6ba643e7cc31
Source dataset
uspto-grants-2014_10
Patent number
US08853409B2

Reaction notes

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