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Water → HCID 390821, compound

HRID 534052
Notes
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Reaction equation

HRID 534052 reaction equation
[OH2:1].Cl.O[NH2:4].C(=O)([O-])[O-].[Na+].[Na+].[O:11]1[C:15]2([CH2:20][CH2:19][CH2:18][CH2:17][CH2:16]2)[O:14][CH2:13][C@@H:12]1[CH:21]=O>C1COCC1>[O:11]1[C:15]2([CH2:20][CH2:19][CH2:18][CH2:17][CH2:16]2)[O:14][CH2:13][C@@H:12]1[CH:21]=[N:4][OH:1]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 962WaterHCID 10340Sodium CarbonateHCID 443297Hydroxyamine hydrochlorideHCID 10855919(R)-1,4-Dioxaspiro(4.5)decane-2-carboxaldehyde

Product 1

HCID 390821HCID 390821, compoundYield 99%

Reagents, catalysts & solvents 1

HCID 8028
Tetrahydrofuran
Solvent
2×

Procedure

To 1000 mL of DI water was added hydroxyl amine hydrochloride (51.0 g, 734 mmol) and the mixture 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) in 800 mL of THF was added in 1 portion. The reaction was stirred for 4 hours and poured into a 4 L separatory funnel and the layers were 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 MgSOa, 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. additionwas added in 1 portion
  3. stirringThe reaction was stirred for 4 hours
  4. additionpoured into a 4 L separatory funnel
  5. customthe layers were separated
  6. extractionThe aqueous layer was extracted twice with MTBE (about 3000 mL total)
  7. washThe combined organic layers were washed with water (700 mL) and brine (300 mL)
  8. customdried over MgSOa
  9. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-d61c80f1bd5a4df19abcd9efb70acdcd
Source dataset
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08853409B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes