Water → HCID 58210237, compound

HRID 1795313Notes

Reaction equation

HRID 1795313 reaction equation
[C:1]1([CH2:7][O:8][CH2:9][CH2:10][O:11][CH2:12][CH2:13][CH:14]([C:20](OCC)=[O:21])[C:15](OCC)=[O:16])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[H-].[H-].[H-].[H-].[Li+].[Al+3].O.[OH-].[Na+]>C1(C)C=CC=CC=1>[C:1]1([CH2:7][O:8][CH2:9][CH2:10][O:11][CH2:12][CH2:13][CH:14]([CH2:15][OH:16])[CH2:20][OH:21])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1

Participants

6

Procedure

C6H5—CH2O—CH2CH2OCH2CH2—CH(COOC2H5)2 (5 g) from Step B was dissolved in 200 ml of toluene and 29.5 ml of LiAlH4 (1 M in THF) was added at 0–5° C. After stirring overnight at room temperature, 1 ml of water was added followed by 1.0 ml of 15% NaOH and 3.0 ml of water. The insoluble material was filtered and the filtrate was evaporated to dryness. The product was purified by flash chromatography on a silica gel column eluted with ethyl acetate. Combined fractions were evaporated to dryness. The final product was dried under vacuum overnight.

Workup

  1. filtrationThe insoluble material was filtered
  2. customthe filtrate was evaporated to dryness
  3. customThe product was purified by flash chromatography on a silica gel column
  4. washeluted with ethyl acetate
  5. customCombined fractions were evaporated to dryness
  6. dry with materialThe final product was dried under vacuum overnight

Sources & evidence

ORD record
ord-40a8b385c42b414883abc511bcffa0ce
Source dataset
uspto-grants-2006_04
Patent number
US07026440B2

Reaction notes

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