2-Indanone → HCID 70490180, compound

HRID 1248054Notes

Reaction equation

[CH2:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3][C:2]1=O.[ClH:11].[CH3:12][O:13][C:14](=[O:18])[C@H:15]([CH3:17])[NH2:16]>>[ClH:11].[CH3:12][O:13][C:14](=[O:18])[C@H:15]([CH3:17])[NH:16][CH:2]1[CH2:3][C:4]2[C:9](=[CH:8][CH:7]=[CH:6][CH:5]=2)[CH2:1]1

Participants

Reactant 2

HCID 119832-Indanone

HCID 2733257Alanine methyl ester hydrochloride

Product 1

HCID 70490180HCID 70490180, compound

Procedure

By a procedure similar to that described in Reference Example 81, 2-indanone and L-alanine methyl ester hydrochloride give N-(2-indanyl)-L-alanine methyl ester hydrochloride. Melting point: 215° C.

Sources & evidence

ORD record: ord-505690be788840aaa618fcf50af56c09
Source dataset: uspto-grants-1985_06
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04521607

Reaction notes

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