Diethyl Ether → HCID 44217645, compound

HRID 2074522Notes

Reaction equation

HRID 2074522 reaction equation
[CH2:1]([N:8]1[C:16]2[C:11](=[CH:12][C:13]([O:17][CH3:18])=[CH:14][CH:15]=2)[C:10]([C:19](OCC2C=CC=CC=2)=[O:20])=[N:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(OCC)C.[H-].[H-].[H-].[H-].[Li+].[Al+3]>O1CCCC1>[CH2:1]([N:8]1[C:16]2[C:11](=[CH:12][C:13]([O:17][CH3:18])=[CH:14][CH:15]=2)[C:10]([CH2:19][OH:20])=[N:9]1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

5

Reactant 3

HCID 3283Diethyl EtherHCID 21226445Aluminium lithium hydrideHCID 66846925HCID 66846925, compound

Product 1

HCID 44217645HCID 44217645, compoundYield 104.4%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

To a solution of benzyl 1-benzyl-5-methoxy-1H-indazole-3-carboxylate (17.7 g; 0.05 mol), diethyl ether (100 ml) and tetrahydrofuran (THF) (170 ml) stirred at room temperature was slowly added LiAlH4 (3.8 g; 0.1 mol). Once the addition was complete, the suspension was stirred at reflux for 24 hours. The reaction was stopped by destroying the excess LiAlH4 via addition of water (40 ml) and 5N NaOH (10 ml). The organic phase was separated out and the solvent was evaporated off under reduced pressure. The crude residue obtained was purified by crystallization from 95° ethanol to give 14 g of (1-benzyl-5-methoxy-1H-indazol-3-yl)methanol with a melting point of 97-98° C.

Workup

  1. additionOnce the addition
  2. temperatureat reflux for 24 hours
  3. customby destroying the excess LiAlH4
  4. additionvia addition of water (40 ml) and 5N NaOH (10 ml)
  5. customThe organic phase was separated out
  6. customthe solvent was evaporated off under reduced pressure
  7. customThe crude residue obtained
  8. customwas purified by crystallization from 95° ethanol

Sources & evidence

ORD record
ord-d20de820f40a48a98001cc6d70d523b5
Source dataset
uspto-grants-2011_04
Patent number
US07919518B2

Reaction notes

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