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Ammonium Chloride → HCID 69211802, compound

HRID 2214239
Notes
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Reaction equation

HRID 2214239 reaction equation
[Li+].CC([N-]C(C)C)C.[CH2:9]([O:11][C:12](=[O:37])[CH2:13][CH2:14][CH2:15][CH2:16][S:17][C:18]([C:31]1[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=1)([C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1)[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1)[CH3:10].Br[CH2:39][C:40]([O:42][C:43]([CH3:46])([CH3:45])[CH3:44])=[O:41].[Cl-].[NH4+]>C1COCC1.CCOCC.CN(P(N(C)C)(N(C)C)=O)C>[CH2:9]([O:11][C:12](=[O:37])[CH:13]([CH2:14][CH2:15][CH2:16][S:17][C:18]([C:31]1[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=1)([C:19]1[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=1)[C:25]1[CH:26]=[CH:27][CH:28]=[CH:29][CH:30]=1)[CH2:39][C:40]([O:42][C:43]([CH3:46])([CH3:45])[CH3:44])=[O:41])[CH3:10]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

8

Reactant 4

HCID 25517Ammonium ChlorideHCID 79177tert-Butyl bromoacetateHCID 2724682Lithium diisopropylamideHCID 69224758HCID 69224758, compound

Product 1

HCID 69211802HCID 69211802, compound

Reagents, catalysts & solvents 3

HCID 3283
Diethyl Ether
Solvent
HCID 8028TetrahydrofuranSolvent2×
HCID 12679HexamethylphosphoramideSolvent

Conditions

Temperature
-40 °C

Procedure

To a solution of LDA (2M, 9.1 mL, 18.17 mmol) at −70° C. was added HMPA(10 mL) followed by the drop wise addition of a solution of the compound of example 27 (6.12 g, 15.14 mmol) in anhydrous THF (10 mL). The reaction mixture was allowed to warm up to −40° C. and was stirred for another 30 minutes, after which, a solution of tert-butyl bromoacetate (2.5 mL, 16.65 mmol) in anhydrous THF (10 mL) was added. The reaction mixture was stirred for 1 h at the same temperature and then allowed to warm up to room temperature followed by stirring for 24 h. The reaction mixture was portioned between ether and saturated ammonium chloride. The water phase was extracted several times with ether. The recombined organic layer was washed with brine, dried, filtered and evaporated. Silica gel chromatography using 5% ethyl acetate in hexanes provided the product as a light yellow oil. 1H-NMR(CDCl3, 400 MH: 1.24(t, J=7.1 Hz, 3H); 1.43(s, 9H); 1.40–1.57(m, 4H); 2.15(m, 2H); 2.24(m, 1H); 2.58(m, 2H); 4.12(q, J=7.1 Hz, 2H), 7.19–7.23, 7.26–7.30, 7.41(m, 15H).

Workup

  1. stirringThe reaction mixture was stirred for 1 h at the same temperature
  2. temperatureto warm up to room temperature
  3. stirringby stirring for 24 h
  4. extractionThe water phase was extracted several times with ether
  5. washThe recombined organic layer was washed with brine
  6. customdried
  7. filtrationfiltered
  8. customevaporated

Sources & evidence

ORD record
ord-9e075e6494f64081b985da2f0e4f6994
Source dataset
uspto-grants-2006_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07105539B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes