Toluene → Ethyl 2,2-dimethoxyethylcarbamate

HRID 2415648Notes

Reaction equation

HRID 2415648 reaction equation
[CH3:1][O:2][CH:3]([O:6][CH3:7])[CH2:4][NH2:5].C1(C)C=CC=CC=1.[OH-].[Na+].Cl[C:18]([O:20][CH2:21][CH3:22])=[O:19]>O>[CH3:1][O:2][CH:3]([O:6][CH3:7])[CH2:4][NH:5][C:18](=[O:19])[O:20][CH2:21][CH3:22]

Participants

6

Conditions

Temperature
10 °C

Procedure

A two-liter, three-necked round bottom flask was fitted with a 125-mL addition funnel and a digital thermometer probe. To this flask was added 65 g (618 mmol) of aminoacetaldehyde dimethyl acetal, 310 mL of toluene, and a solution of 27.8 g (695 mmol) of NaOH in 155 mL of water. This reaction mixture was cooled to 10° C. via ice bath. Ethyl chloroformate (59.1 mL, 618 mmol) was then added dropwise to the reaction mixture via addition funnel over a 15-20 minute period making sure the reaction temperature stayed near 10° C. Once addition was complete the reaction was stirred at room temperature for two hours. The aqueous layer was then separated, saturated with solid sodium chloride, and extracted with 3×50 mL of toluene. The toluene layers were combined, dried over magnesium sulfate, filtered, and concentrated in vacuo.

Workup

  1. customA two-liter, three-necked round bottom flask was fitted with a 125-mL addition funnel
  2. customstayed near 10° C
  3. additionOnce addition
  4. customThe aqueous layer was then separated, saturated with solid sodium chloride
  5. extractionextracted with 3×50 mL of toluene
  6. dry with materialdried over magnesium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-d7a64c0b00fd4c87a108e624cd95bb86
Source dataset
uspto-grants-2004_11
Patent number
US06821964B2

Reaction notes

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