Ethyl 1,4-dioxaspiro(4.5)decane-8-carboxylate → 1,4-Dioxaspiro(4.5)decane-8-carbaldehyde

HRID 1821636Notes

Reaction equation

HRID 1821636 reaction equation
[H-].C([Al+]CC(C)C)C(C)C.C([O:13][C:14]([CH:16]1[CH2:25][CH2:24][C:19]2([O:23][CH2:22][CH2:21][O:20]2)[CH2:18][CH2:17]1)=O)C>C1(C)C=CC=CC=1>[O:20]1[C:19]2([CH2:24][CH2:25][CH:16]([CH:14]=[O:13])[CH2:17][CH2:18]2)[O:23][CH2:22][CH2:21]1

Participants

4

Procedure

Diisobutyl aluminium hydride (1.5 M solution in toluene, 102 ml, 153 mmole) was added dropwise to a solution of 1,4-dioxa-spiro[4.5]decane-8-carboxylic acid ethyl ester 10 (32.13 g, 150 mmole) in absolute toluene (160 ml) under argon at −70° to −65° C. and stirred for 30 minutes. The reaction mixture was then quenched at −70° to −60° C. by adding methanol (80 ml). The reaction solution was heated to RT, sodium chloride solution (100 ml) was added, and the reaction solution was suction filtered through diatomaceous earth. The diatomaceous earth was washed twice with ethyl acetate, and the aqueous solution was separated and extracted twice with ethyl acetate. The combined organic extracts were washed with saturated sodium chloride solution, dried over sodium sulfate and concentrated by evaporation in vacuo.

Workup

  1. customThe reaction mixture was then quenched at −70° to −60° C.
  2. additionby adding methanol (80 ml)
  3. additionsodium chloride solution (100 ml) was added
  4. filtrationfiltered through diatomaceous earth
  5. washThe diatomaceous earth was washed twice with ethyl acetate
  6. customthe aqueous solution was separated
  7. extractionextracted twice with ethyl acetate
  8. washThe combined organic extracts were washed with saturated sodium chloride solution
  9. dry with materialdried over sodium sulfate
  10. concentrationconcentrated by evaporation in vacuo

Sources & evidence

ORD record
ord-0421fe8886b7460e9d41fbfefe787cc8
Source dataset
uspto-grants-2009_10
Patent number
US07608619B2

Reaction notes

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