Hydrochloric Acid → HCID 53655601, compound

HRID 2395394Notes

Reaction equation

HRID 2395394 reaction equation
C[O:2][C:3](=[O:26])[CH2:4][CH2:5][CH2:6][CH2:7][CH:8]1[O:12][C:11]2[CH:13]=[C:14]([CH:17]([OH:25])[CH2:18][CH2:19][C:20]3[S:21][CH:22]=[CH:23][CH:24]=3)[CH:15]=[CH:16][C:10]=2[O:9]1.[OH-].[Li+].Cl>O.C1COCC1>[OH:25][CH:17]([C:14]1[CH:15]=[CH:16][C:10]2[O:9][CH:8]([CH2:7][CH2:6][CH2:5][CH2:4][C:3]([OH:26])=[O:2])[O:12][C:11]=2[CH:13]=1)[CH2:18][CH2:19][C:20]1[S:21][CH:22]=[CH:23][CH:24]=1

Participants

6

Reactant 3

HCID 313Hydrochloric AcidHCID 3939Lithium HydroxideHCID 18972191HCID 18972191, compound

Product 1

HCID 53655601HCID 53655601, compoundYield 99%

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 8028TetrahydrofuranSolvent

Conditions

Temperature
23 °C

Procedure

A mixture of (±)-methyl-5-[[6-(1-hydroxy-3-(2-thienyl)propyl-1,3-benzodioxolyl]pentanoate (Compound F, 35 mg, 0.093 mmol) and lithium hydroxide (0.37 mL of a 0.5N solution in H2O, 0.186 mmol) in THF (0.74 mL) was stirred at 23° C. for 16 hours. The mixture was acidified with 1N HCl and extracted with EtOAc. The organic portion was dried (MgSO4) filtered and concentrated in vacuo. Flash column chromatography (silica gel, 100% EtOAc) afforded 33.3 mg (99%) of the title compound. 1H NMR (300 MHz, CDCl3) δ 12.0 (brs, 1H), 7.14 (d, J=5.1 Hz, 1H), 7.00 (s, 1H), 6.93 (dd, J=3.3, 5.1 Hz, 1H), 6.83 (d, J=3.3 Hz, 1H), 6.59 (s, 1H), 5.91 (s, 2H), 4.87-4.92 (m, 1H), 2.97 (t, J=5.4 Hz, 2H), 2.43-2.47 (m, 2H), 2.32 (t, J=6.9 Hz, 2H), 1.86-2.18 (m, 2H), 1.44-1.64 (m, 5H).

Workup

  1. extractionextracted with EtOAc
  2. dry with materialThe organic portion was dried (MgSO4)
  3. filtrationfiltered
  4. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-5da89498effa40d8b0edca7a47ddd063
Source dataset
uspto-grants-1998_09
Patent number
US05814657

Reaction notes

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