4-Chloro-3,5-dinitrobenzotrifluoride → HCID 59293622, compound

HRID 2059784Notes

Reaction equation

HRID 2059784 reaction equation
[C:1]([O:5][C:6]([N:8]1[CH2:12][CH2:11][C@@H:10]([OH:13])[CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].CC(C)([O-])C.[K+].Cl[C:21]1[C:26]([N+:27]([O-:29])=[O:28])=[CH:25][C:24]([C:30]([F:33])([F:32])[F:31])=[CH:23][C:22]=1[N+:34]([O-:36])=[O:35]>O1CCCC1.COC(C)(C)C>[C:1]([O:5][C:6]([N:8]1[CH2:12][CH2:11][C@@H:10]([O:13][C:21]2[C:22]([N+:34]([O-:36])=[O:35])=[CH:23][C:24]([C:30]([F:33])([F:31])[F:32])=[CH:25][C:26]=2[N+:27]([O-:29])=[O:28])[CH2:9]1)=[O:7])([CH3:4])([CH3:2])[CH3:3]

Participants

6

Reactant 3

HCID 98094-Chloro-3,5-dinitrobenzotrifluoride2×HCID 6544479tert-Butyl (3R)-3-hydroxypyrrolidine-1-carboxylate2×HCID 23665647Potassium tert-butoxide

Product 1

HCID 59293622HCID 59293622, compound

Reagents, catalysts & solvents 2

HCID 8028TetrahydrofuranSolventHCID 15413tert-Butyl methyl etherSolvent

Procedure

(R)-3-Hydroxypyrrolidine-1-carboxylic acid tert-butyl ester (compound 20) is de-protonated with potassium tert-butoxide (KOtBu) in tetrahydrofuran (THF). The resulting anion is reacted 2-chloro-1,3-dinitro-5-trifluoromethylbenzene (compound 2) in tert-butyl methyl ether (MTBE)/THF. When the reaction is complete, the reaction mixture is quenched with water and partitioned with more MTBE. The organic layer is washed with brine and water and concentrated on a rotary evaporator. The solid concentrate is re-dissolved in methanol and re-precipitated with water. The resulting precipitate is filtered and dried to afford (R)-3-(2,6-dinitro-4-trifluoromethylphenoxy)pyrrolidine-1-carboxylic acid tert-butyl ester which can be used in the next step without further purification. This reaction has been carried out at a scale using 4.2 Kg of compound 2.

Workup

  1. customthe reaction mixture is quenched with water
  2. custompartitioned with more MTBE
  3. washThe organic layer is washed with brine and water
  4. concentrationconcentrated on a rotary evaporator
  5. concentrationThe solid concentrate
  6. dissolutionis re-dissolved in methanol
  7. customre-precipitated with water
  8. filtrationThe resulting precipitate is filtered
  9. customdried

Sources & evidence

ORD record
ord-c06c72fbd8d84eaeb1e4cf7495ffa5dd
Source dataset
uspto-grants-2012_10
Patent number
US08278309B2

Reaction notes

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