Dichloromethane → Benzyl N-(3-hydroxypropyl)carbamate

HRID 1922574Notes

Reaction equation

HRID 1922574 reaction equation
[NH2:1][CH2:2][CH2:3][CH2:4][OH:5].C([O-])([O-])=O.[Na+].[Na+].[CH:12]1[CH:17]=[CH:16][C:15]([CH2:18][O:19][C:20](Cl)=[O:21])=[CH:14][CH:13]=1.C(Cl)Cl>C1COCC1.O>[OH:5][CH2:4][CH2:3][CH2:2][NH:1][C:20](=[O:21])[O:19][CH2:18][C:15]1[CH:16]=[CH:17][CH:12]=[CH:13][CH:14]=1

Participants

7

Reactant 4

HCID 6344DichloromethaneHCID 90863-Amino-1-propanolHCID 10340Sodium CarbonateHCID 10387Benzyl chloroformate

Product 1

HCID 562256Benzyl N-(3-hydroxypropyl)carbamateYield 90.5%

Reagents, catalysts & solvents 2

HCID 962WaterSolvent2×HCID 8028TetrahydrofuranSolvent

Procedure

To a mixture of 3-aminopropan-1-ol (5.0 g, 67 mmol), Na2CO3 (8.8 g, 83 mmol) in THF (40 mL) and H2O (130 mL) at 0° C. was added Cbz-Cl (14.8 g, 87 mmol). The reaction mixture was stirred (RT, 1 h). Water (500 mL) and CH2Cl2 (500 mL) were added, and the layers were separated. The organic layer was dried over MgSO4 and concentrated under reduced pressure. The residue was purified by silica chromatography (PE:EA, 5:1) to afford benzyl 3-hydroxypropylcarbamate as a white solid (12.6 g, 90.5%).

Workup

  1. customthe layers were separated
  2. dry with materialThe organic layer was dried over MgSO4
  3. concentrationconcentrated under reduced pressure
  4. customThe residue was purified by silica chromatography (PE:EA, 5:1)

Sources & evidence

ORD record
ord-f00f99db3c1e47939db9dab817ecd3cb
Source dataset
uspto-grants-2012_05
Patent number
US08173831B2

Reaction notes

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