Potassium borohydride → HCID 178435403, compound

HRID 597016Notes

Reaction equation

HRID 597016 reaction equation
[O:1]=[C:2]([O:8][C:9]1[CH:10]=[C:11]2[C:15](=[C:16]([Cl:19])[C:17]=1[Cl:18])[CH2:14][CH:13]([CH2:20][CH3:21])[CH2:12]2)[C:3]1[NH:7][N:6]=[N:5][N:4]=1.[BH4-].[K+]>O>[OH:1][CH:2]([O:8][C:9]1[CH:10]=[C:11]2[C:15](=[C:16]([Cl:19])[C:17]=1[Cl:18])[CH2:14][CH:13]([CH2:20][CH3:21])[CH2:12]2)[C:3]1[NH:7][N:6]=[N:5][N:4]=1

Participants

4

Reactant 2

HCID 4192641Potassium borohydrideHCID 178435402HCID 178435402, compound

Product 1

HCID 178435403HCID 178435403, compound

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

5-(1-Hydroxy-2-ethyl-6,7-dichloro-5-indanyloxymethyl)tetrazole is prepared following substantially the same procedure described in Example 1, using the following substances: 5-(1-oxo-2-ethyl-6,7-dichloro-5-indanyloxymethyl)tetrazole (6.54 g., 0.02 mole); potassium borohydride (2.0 g.); and water (200 ml.).

Sources & evidence

ORD record
ord-69b524f83d57484d85beb6b2ca53d7c3
Source dataset
uspto-grants-1977_03
Patent number
US04012524

Reaction notes

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