Trifluoroacetic acid → HCID 9903131, compound

HRID 844640Notes

Reaction equation

HRID 844640 reaction equation
C([O:5][C:6]([CH2:8][C:9]1[CH:14]=[CH:13][C:12]([O:15][C:16]([C:18]2[CH:27]=[CH:26][C:25]3[C:24](=[O:28])[CH2:23][CH2:22][C:21]([CH3:30])([CH3:29])[C:20]=3[CH:19]=2)=[O:17])=[CH:11][CH:10]=1)=[O:7])(C)(C)C.FC(F)(F)C(O)=O.C(OCC)(=O)C>ClCCl>[C:6]([CH2:8][C:9]1[CH:10]=[CH:11][C:12]([O:15][C:16]([C:18]2[CH:27]=[CH:26][C:25]3[C:24](=[O:28])[CH2:23][CH2:22][C:21]([CH3:30])([CH3:29])[C:20]=3[CH:19]=2)=[O:17])=[CH:13][CH:14]=1)([OH:7])=[O:5]

Participants

5

Procedure

A solution of 8,8-dimethyl-5-oxo-5,6,7,8-tetrahydro-naphthalene-2-carboxylic acid 4-(tert-butoxycarbonylmethyl)phenyl Ester (Compound 19, 0.11 g, 0.229 mmol) in dichloromethane (2 mL) was treated with trifluoroacetic acid (0.85 mL and stirred at ambient temperature for 2.5 h. The volatiles were distilled off in vacuo and the residue was diluted with water and extracted with ethyl acetate (×3). The combined organic phase was dried over anhydrous sodium sulfate, filtered and evaporated in vacuo to afford a solid which was subjected to flash column chromatography over silica gel (230-400 mesh) using ethyl acetate as the eluent to afford the title compound (0.024 g, 25%).

Workup

  1. distillationThe volatiles were distilled off in vacuo
  2. additionthe residue was diluted with water
  3. extractionextracted with ethyl acetate (×3)
  4. dry with materialThe combined organic phase was dried over anhydrous sodium sulfate
  5. filtrationfiltered
  6. customevaporated in vacuo
  7. customto afford a solid which

Sources & evidence

ORD record
ord-f8b5a0ecfa604fba8cfb88a40a5ab55d
Source dataset
uspto-grants-2002_04
Patent number
US06380256B1

Reaction notes

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