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Triethylamine → (2S,4R)-2-(2-hydroxyethyloxymethyl)-4-methanesulfonyloxy-1-(4-nitrobenzyloxycarbonyl)pyrrolidine

HRID 703573
Notes
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Reaction equation

HRID 703573 reaction equation
ClC(OCC(C)C)=O.[C:9]([CH2:12][O:13][CH2:14][C@@H:15]1[CH2:19][C@@H:18]([O:20][S:21]([CH3:24])(=[O:23])=[O:22])[CH2:17][N:16]1[C:25]([O:27][CH2:28][C:29]1[CH:34]=[CH:33][C:32]([N+:35]([O-:37])=[O:36])=[CH:31][CH:30]=1)=[O:26])(O)=[O:10].C(N(CC)CC)C>O1CCCC1>[OH:10][CH2:9][CH2:12][O:13][CH2:14][C@@H:15]1[CH2:19][C@@H:18]([O:20][S:21]([CH3:24])(=[O:23])=[O:22])[CH2:17][N:16]1[C:25]([O:27][CH2:28][C:29]1[CH:30]=[CH:31][C:32]([N+:35]([O-:37])=[O:36])=[CH:33][CH:34]=1)=[O:26]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 8471TriethylamineHCID 62365Isobutyl chloroformateHCID 18631935(2S,4R)-2-(carboxymethyloxymethyl)-4-methanesulfonyloxy-1-(4-nitrobenzyloxycarbonyl)pyrrolidine

Product 1

HCID 18641547(2S,4R)-2-(2-hydroxyethyloxymethyl)-4-methanesulfonyloxy-1-(4-nitrobenzyloxycarbonyl)pyrrolidineYield 90.4%

Reagents, catalysts & solvents 1

HCID 8028
Tetrahydrofuran
Solvent
2×

Procedure

A solution of isobutyl chloroformate (1.08 ml) in tetrahydrofuran (3 ml) was dropwise added to a solution of (2S,4R)-2-(carboxymethyloxymethyl)-4-methanesulfonyloxy-1-(4-nitrobenzyloxycarbonyl)pyrrolidine (2.4 g) and triethylamine (1.55 ml) in tetrahydrofuran (50 ml) at -10°~5° C., and the mixture was stirred at the same temperature for 0.5 hour. The precipitate was filtered off. To the filtrate was added sodium borohydride (0.7 g) and water (30 ml) at 0° C. After 1 hour, glacial acetic acid (3 ml) was added to the mixture. The mixture was poured into a mixture of water (50 ml) and ethyl acetate (50 ml). The organic layer was separated, washed with water, saturated aqueous sodium hydrogen carbonate and brine in turn, dried over magnesium sulfate, and concentrated under reduced pressure to give a syrup. The syrup was subjected to a column chromatography on silica gel (30 g) and eluted with a mixture of methanol and chloroform (5:95 V/V) to give (2S,4R)-2-(2-hydroxyethyloxymethyl)-4 -methanesulfonyloxy-1-(4-nitrobenzyloxycarbonyl)pyrrolidine (2.10 g).

Workup

  1. filtrationThe precipitate was filtered off
  2. additionTo the filtrate was added sodium borohydride (0.7 g) and water (30 ml) at 0° C
  3. waitAfter 1 hour
  4. additionglacial acetic acid (3 ml) was added to the mixture
  5. additionThe mixture was poured into a mixture of water (50 ml) and ethyl acetate (50 ml)
  6. customThe organic layer was separated
  7. washwashed with water, saturated aqueous sodium hydrogen carbonate and brine in turn
  8. dry with materialdried over magnesium sulfate
  9. concentrationconcentrated under reduced pressure
  10. customto give a syrup
  11. washeluted with a mixture of methanol and chloroform (5:95 V/V)

Sources & evidence

ORD record
ord-1df70fa7d66c4c8ba95d9784357c262a
Source dataset
uspto-grants-1991_01
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04983596

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes