Acetyl chloride → HCID 53685052, compound

HRID 1598563Notes

Reaction equation

HRID 1598563 reaction equation
[CH2:1]([S:5]([NH:8][CH:9]1[CH2:17][C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[CH2:10]1)(=[O:7])=[O:6])[CH2:2][CH2:3][CH3:4].[C:18](Cl)(=[O:20])[CH3:19]>>[CH2:1]([S:5]([NH:8][CH:9]1[CH2:17][C:16]2[C:11](=[CH:12][CH:13]=[C:14]([C:18](=[O:20])[CH3:19])[CH:15]=2)[CH2:10]1)(=[O:7])=[O:6])[CH2:2][CH2:3][CH3:4]

Participants

3

Reactant 2

HCID 6367Acetyl chlorideHCID 53680058HCID 53680058, compound

Product 1

HCID 53685052HCID 53685052, compound

Procedure

2-n-Butylsulfonylaminoindane and acetyl chloride were treated in the same manner as in Example 31-(2) to obtain 2-n-butylsulfonylamino-5-acetylindane.

Sources & evidence

ORD record
ord-61d00375c8f64a18aaaabbdb75972e41
Source dataset
uspto-grants-1998_04
Patent number
US05739132

Reaction notes

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