Sodium Hydroxide → HCID 13243718, compound

HRID 1389190Notes

Reaction equation

HRID 1389190 reaction equation
[CH2:1]([O:8][C:9]1[CH:10]=[C:11](/[C:23](/[CH3:30])=[CH:24]\[C:25](OCC)=[O:26])[CH:12]=[C:13]([O:15][CH2:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[CH:14]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-].[Cl-].[Al+3].[Cl-].[Cl-].[OH-].[Na+]>CCOCC.O>[CH2:16]([O:15][C:13]1[CH:12]=[C:11]([CH:23]([CH3:30])[CH2:24][CH2:25][OH:26])[CH:10]=[C:9]([O:8][CH2:1][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)[CH:14]=1)[C:17]1[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=1

Participants

7

Procedure

A solution of ethyl 3-(3,5-dibenzyloxyphenyl)crotonate (24.1 g., 60 mM) in ether (250 ml.) is added to a mixture of lithium aluminum hydride (3.42 g., 90 mM) and ether (250 ml.). Aluminum chloride (0.18 g., 1.35 mM) is added and the mixture refluxed for 12 hours and then cooled. Water (3.4 ml.), sodium hydroxide (3.4 ml. of 6 N) and water (10 ml.) are then added successively to the reaction mixture. The inorganic salts which precipitate are filtered off and the filtrate is then concentrated in vacuo to give the desired alcohol as an oil--2.4 g. (98%).

Workup

  1. temperaturethe mixture refluxed for 12 hours
  2. temperaturecooled
  3. filtrationThe inorganic salts which precipitate are filtered off
  4. concentrationthe filtrate is then concentrated in vacuo

Sources & evidence

ORD record
ord-13d53110ee3e49629b21ea8e52cba754
Source dataset
uspto-grants-1981_01
Patent number
US04243674

Reaction notes

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