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Hydrochloric Acid → tert-Butyl (2S,3S)-3-(tert-butyldimethylsilyloxy)-1-(3-fluorophenyl)-4-hydroxybutan-2-ylcarbamate

HRID 20007
Notes
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Reaction equation

HRID 20007 reaction equation
[Si:1]([O:8][C@H:9]([CH2:26][O:27][Si](C(C)(C)C)(C)C)[C@@H:10]([NH:19][S@](C(C)(C)C)=O)[CH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[C:14]([F:18])[CH:13]=1)([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2].Cl.COC1C=CC(C=O)=CC=1.[O:46](C(OC(C)(C)C)=O)[C:47]([O:49][C:50]([CH3:53])([CH3:52])[CH3:51])=O>C(OCC)C.CCO>[Si:1]([O:8][C@H:9]([CH2:26][OH:27])[C@@H:10]([NH:19][C:47](=[O:46])[O:49][C:50]([CH3:53])([CH3:52])[CH3:51])[CH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[C:14]([F:18])[CH:13]=1)([C:4]([CH3:5])([CH3:7])[CH3:6])([CH3:2])[CH3:3]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 4

HCID 313Hydrochloric AcidHCID 312444-MethoxybenzaldehydeHCID 90495Di-tert-butyl dicarbonateHCID 67305247(S)-N-((2S,3S)-3,4-bis(tert-butyldimethylsilyloxy)-1-(3-fluorophenyl)butan-2-yl)-2-methylpropane-2-sulfinamide

Product 1

HCID 86614117tert-Butyl (2S,3S)-3-(tert-butyldimethylsilyloxy)-1-(3-fluorophenyl)-4-hydroxybutan-2-ylcarbamate

Reagents, catalysts & solvents 2

HCID 702EthanolSolventHCID 3283Diethyl EtherSolvent

Conditions

Temperature
0 °C

Procedure

To a 500 mL RBF containing (S)—N-((2S,3S)-3,4-bis(tert-butyldimethylsilyloxy)-1-(3-fluorophenyl)butan-2-yl)-2-methylpropane-2-sulfinamide (2.600 g, 4.9 mmol) was added EtOH (25 ml) and the mixture was allowed to stir at 0° C. for 15 min. At this time, HCl (4N in dioxane) (3.7 ml, 15 mmol) was added via syringe. The reaction was monitored at 1 h by LC/MS 76877-2-1 and tlc (100% EtOAC amino bis TBS; Rf=0.80 UV active stains orange to anisaldehyde amine with primary alcohol deprotected Rf=0.45 to 0.1 streak, UV active and stains white to anisaldehyde). The reaction was allowed to stir for 3 h at 0° C. and then TEA (4.1 ml, 29 mmol) was added fast dropwise and a white solid formed. An LC/Ms was obtained to confirm that the secondary TBS ether was not removed during the TEA neutralization process. Approximately 15 mL of EtOH were removed by rotary evaporator and then DCM (10 mL) was added and the solid went into solution. At this time, (BOC)2O (2.3 ml, 9.8 mmol) was added in one portion and the reaction was allowed to stir for 1 h and then poured into diethyl ether (300 ml). The organic layer was washed with ammonium chloride (3×150 mL, sat) and brine. The organic layer was dried with magnesium sulfate, filtered and concentrated to give a colorless crude oil. The desired product has an Rf=0.40 in 35% EtOAc in hexanes, UV active, stains white to anisaldehyde and purple to moly stain. The crude oil was purified on a 120 g Isco column (10 to 35% EtOAc in hexanes) to give the title compound as a colorless oil.

Workup

  1. stirringto stir for 3 h at 0° C.
  2. customa white solid formed
  3. customAn LC/Ms was obtained
  4. customwas not removed during the TEA neutralization process
  5. customApproximately 15 mL of EtOH were removed by rotary evaporator
  6. additionDCM (10 mL) was added
  7. stirringto stir for 1 h
  8. washThe organic layer was washed with ammonium chloride (3×150 mL, sat) and brine
  9. dry with materialThe organic layer was dried with magnesium sulfate
  10. filtrationfiltered
  11. concentrationconcentrated
  12. customto give a colorless crude oil

Sources & evidence

ORD record
ord-4bc2f48018cb4f2fa295acd114602b09
Source dataset
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07745484B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes