Water → HCID 12466834, compound

HRID 1679433Notes

Reaction equation

HRID 1679433 reaction equation
[OH:1][CH2:2][CH2:3][N:4]1[CH2:8][CH2:7][O:6][CH:5]1[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1.[Mg].[CH3:16][O:17][C:18]1[CH:19]=[C:20]([CH:23]=[CH:24][CH:25]=1)[CH2:21]Cl.O>CCOCC>[OH:1][CH2:2][CH2:3][N:4]([CH:5]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)[CH2:21][C:20]1[CH:23]=[CH:24][CH:25]=[C:18]([O:17][CH3:16])[CH:19]=1)[CH2:8][CH2:7][OH:6]

Participants

6

Procedure

A solution of 3-(2-hydroxyethyl)-2-phenyloxazolidine (11.0 g) in anhydrous ether (30 ml) is added dropwise with stirring to Grignard reagent which is prepared from magnesium turnings (3.3 g) and m-methoxybenzyl chloride (20.7 g) in anhydrous ether (150 ml), and the mixture is refluxed for 3 hours. After the reaction, the reaction mixture is decomposed by adding water thereto. The ether layer is separated and extracted with 10% hydrochloric acid (100 ml). The hydrochloric acid layer is made alkaline with ammonia and extracted with ether. The ether layer is dried over anhydrous sodium sulfate, and the solvent is distilled off to give crude dl-N,N-bis(2-hydroxyethyl)-2-(3-methoxyphenyl)-1-phenylethylamine (12.7 g) as an oily substance. When this substance is recrystallized from ethanol, it shows a melting point of 67°-69° C.

Workup

  1. temperaturethe mixture is refluxed for 3 hours
  2. customAfter the reaction
  3. customThe ether layer is separated
  4. extractionextracted with 10% hydrochloric acid (100 ml)
  5. extractionextracted with ether
  6. dry with materialThe ether layer is dried over anhydrous sodium sulfate
  7. distillationthe solvent is distilled off

Sources & evidence

ORD record
ord-c6203a5dd0a94b86bea703474d3cbca6
Source dataset
uspto-grants-1978_03
Patent number
US04080453

Reaction notes

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