Reaction #163523

ord-efd9c31ad02147a0b0605978b604591c

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Other1.447 g of P1 were obtained

Procedure

Procedure & NMR Data: 1.5 g (7.9 mmol) of 2-bromo-6-aminophenol, 1.08 ml (0.9 eq, 7.11 mmol) of 1.8-diazabicyclo[5.4.0]undec-7-ene and 3.5 mL of DL-Ethyl 2-bromobutyrate (3 eq, 23.7 mmol)) in 30 mL of 1-Methyl-2-pyrrolidinone were mixed. 1.447 g of P1 were obtained, yield 71%.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08835628B2uspto-grants-2014_09