Hydrochloric Acid → HCID 7023251, compound

HRID 1045160Notes

Reaction equation

HRID 1045160 reaction equation
[NH2:1][C@H:2]([C:7]1[S:8][CH:9]=[CH:10][CH:11]=1)[CH2:3][C:4]([OH:6])=[O:5].[CH2:12]([O:19][C:20](Cl)=[O:21])[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.O1CCOCC1.Cl>[OH-].[Na+]>[CH2:12]([O:19][C:20]([NH:1][C@H:2]([C:7]1[S:8][CH:9]=[CH:10][CH:11]=1)[CH2:3][C:4]([OH:6])=[O:5])=[O:21])[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1

Participants

6

Reactant 4

HCID 313Hydrochloric AcidHCID 10387Benzyl chloroformateHCID 312751,4-DioxaneHCID 86716(S)-3-Amino-3-(thiophen-2-yl)propanoic acid

Product 1

HCID 7023251HCID 7023251, compound

Reagents, catalysts & solvents 1

HCID 14798Sodium HydroxideSolvent

Procedure

(S)-3-amino-3-(thiophen-2-yl)propanoic acid (0.894 g) and benzyloxycarbonyl chloride 0.980 g) were stirred in 2M NaOH (8 mL) and dioxane (26 mL) at 0° C. for 24 hours. The reaction mixture was acidified with concentrated aqueous HCl, extracted twice with ethyl acetate, and the extracts were dried over MgSO4, filtered, concentrated, and chromatographed on silica gel with 50% ethyl acetate/hexanes.

Workup

  1. extractionextracted twice with ethyl acetate
  2. dry with materialthe extracts were dried over MgSO4
  3. filtrationfiltered
  4. concentrationconcentrated
  5. customchromatographed on silica gel with 50% ethyl acetate/hexanes

Sources & evidence

ORD record
ord-716ff2826b41404f88c0a5d9f4e670d9
Source dataset
uspto-grants-2013_10
Patent number
US08563735B2

Reaction notes

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