Hydrochloric Acid → HCID 20358452, compound

HRID 1679699Notes

Reaction equation

HRID 1679699 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]([Cl:12])[C:9]=2[Cl:11])[CH2:4][CH:3]1[CH:18]([CH3:20])[CH3:19].[OH-:21].[Na+].[CH2:23]=O.Cl>O>[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]([Cl:12])[C:9]=2[Cl:11])[CH2:4][C:3]1([CH2:23][OH:21])[CH:18]([CH3:20])[CH3:19]

Participants

6

Procedure

To a solution of (1-oxo-2-isopropyl-6,7-dichloro-5-indanyloxy)acetic acid (3.17 g., 0.01 mole) and sodium hydroxide (0.5 g., 0.0125 mole) in water (90 ml.) is added aqueous formaldehyde (1 ml., 0.012 mole). The resulting solution is stirred at 20°-25° C. for 41/2 days and acidified with hydrochloric acid. There is obtained 2.5 g. of (1-oxo-2-hydroxymethyl-2-isopropyl-6,7-dichloro-5-indanyloxy)acetic acid which melts at 200°-202° C. after recrystallization from ethanol-water.

Workup

  1. customThere is obtained 2.5 g
  2. customof (1-oxo-2-hydroxymethyl-2-isopropyl-6,7-dichloro-5-indanyloxy)acetic acid which melts at 200°-202° C. after recrystallization from ethanol-water

Sources & evidence

ORD record
ord-0d9e5fd9ebb34d61b066203327d5402e
Source dataset
uspto-grants-1978_03
Patent number
US04081554

Reaction notes

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