HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

Water → 4-(4-Methylphenyl)butanol

HRID 1479268
Notes
Print preview

Reaction equation

HRID 1479268 reaction equation
[H-].[Al+3].[Li+].[H-].[H-].[H-].[CH3:7][C:8]1[CH:13]=[CH:12][C:11]([CH2:14][CH2:15][CH2:16][C:17](O)=[O:18])=[CH:10][CH:9]=1.O.[OH-].[Na+]>CCOCC>[CH3:7][C:8]1[CH:13]=[CH:12][C:11]([CH2:14][CH2:15][CH2:16][CH2:17][OH:18])=[CH:10][CH:9]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 962Water2×HCID 14798Sodium HydroxideHCID 782794-p-Tolylbutyric acidHCID 21226445Aluminium lithium hydride

Product 1

HCID 1040094-(4-Methylphenyl)butanol

Reagents, catalysts & solvents 1

HCID 3283Diethyl EtherSolvent
2×

Procedure

To lithium aluminum hydride (427 mg, 11.2 mmol) suspended in dry ether (5 ml) at 0° C. is added 1 g of 4-(4-methylphenyl)butanoic acid (5.614 mmol) dissolved in dry ether (10 ml) over a period of 30 minutes. The reaction mixture is then allowed to warm to room temperature and stirred for 4 hours. Water (0.43 ml), NaOH (15% solution, 0.43 g) and water (1.29 ml) were then added successively and the resulting solution is stirred for 30 minutes. The resulting precipitate is filtered and washed with ether and dried. The filtrate is then concentrated and purified by flash chromatography using ethyl acetate-hexanes as the eluting medium.

Workup

  1. stirringthe resulting solution is stirred for 30 minutes
  2. filtrationThe resulting precipitate is filtered
  3. washwashed with ether
  4. customdried
  5. concentrationThe filtrate is then concentrated
  6. custompurified by flash chromatography

Sources & evidence

ORD record
ord-cc6f07d03f6f4eb9b51fa0bfbbe89f0c
Source dataset
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09408927B2

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes