1,1-Dimethylethyl N-((6-fluoro-4-hydroxy-1,1-dimethyl-2-oxo-naphthalen-3-yl)carbonyl)glycinate → N-((6-Fluoro-4-hydroxy-1,1-dimethyl-2-oxo-naphthalen-3-yl)carbonyl)glycine

HRID 2078058Notes

Reaction equation

HRID 2078058 reaction equation
[F:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[C:8]([CH3:13])([CH3:12])[C:7](=[O:14])[C:6]([C:15]([NH:17][CH2:18][C:19]([O:21]C(C)(C)C)=[O:20])=[O:16])=[C:5]2[OH:26]>C(O)(C(F)(F)F)=O>[F:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[C:8]([CH3:13])([CH3:12])[C:7](=[O:14])[C:6]([C:15]([NH:17][CH2:18][C:19]([OH:21])=[O:20])=[O:16])=[C:5]2[OH:26]

Participants

3

Procedure

A mixture of 1,1-dimethylethyl N-((6-fluoro-4-hydroxy-1,1-dimethyl-2-oxo-naphthalen-3-yl)carbonyl)glycinate (0.6 g, 2 mmol) in 3 mL TFA was stirred at room temperature for 30 minutes. The mixture was concentrated and triturated in ether 20 mL. The solid was filtered, washed with 10 mL ether, and dried under high vacuum to give 0.46 g of the product as an off-white solid. MS m/e=308 (M+H)+. Calculated for C15H14FNO5 307.09.

Workup

  1. concentrationThe mixture was concentrated
  2. customtriturated in ether 20 mL
  3. filtrationThe solid was filtered
  4. washwashed with 10 mL ether
  5. customdried under high vacuum

Sources & evidence

ORD record
ord-a909eb9678f24b57a1ced98eb575b0d7
Source dataset
uspto-grants-2011_04
Patent number
US07928139B2

Reaction notes

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