Chlorine → HCID 20373855, compound

HRID 1834694Notes

Reaction equation

HRID 1834694 reaction equation
[O:1]=[C:2]1[C:10]2[C:5](=[CH:6][C:7]([O:13][CH2:14][C:15]([OH:17])=[O:16])=[C:8]([CH3:12])[C:9]=2[CH3:11])[CH:4]([CH3:18])[CH:3]1[CH2:19][CH3:20].[Cl:21]Cl>Cl.C(O)(=O)C>[O:1]=[C:2]1[C:10]2[C:5](=[CH:6][C:7]([O:13][CH2:14][C:15]([OH:17])=[O:16])=[C:8]([CH3:12])[C:9]=2[CH3:11])[CH:4]([CH3:18])[C:3]1([CH2:19][CH3:20])[Cl:21]

Participants

5

Procedure

By following substantially the procedure described in Example 12, Step B, using as the reactants (1-oxo-2-ethyl-3,6,7-trimethyl-5-indanyloxy)acetic acid (2.76 g., 0.01 mole), glacial acetic acid (50 ml.), chlorine (710 mg., 0.01 mole) and concentrated hydrochloric acid (1 drop) there is obtained (1-oxo-2-ethyl-2-chloro-3,6,7-trimethyl-5-indanyloxy)acetic acid.

Sources & evidence

ORD record
ord-34d7b5fdfe5a428abfe625472e5738c8
Source dataset
uspto-grants-1978_01
Patent number
US04070539

Reaction notes

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