Reaction #7054

ord-7b3ef08a6ec846058fe20b3dbccc2c1d

Reaction equation

[C]=O
carbon monoxide
NS(=O)(=O)c1ccc(Br)s1
5-bromothiophene-2-sulfonamide
CCN(CC)CC
triethyl amine
c1ccc(P(CCCP(c2ccccc2)c2ccccc2)c2ccccc2)cc1
1,3-bis(diphenylphosphino) propane
CCOC(C)=O
ethyl acetate
COC(=O)c1ccc(S(N)(=O)=O)s1
title compound
COC(=O)c1ccc(S(N)(=O)=O)s1
5-(Methoxycarbonyl)thiophene-2-sulfonamide

Conditions

Temperature
100°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    OtherThe organic phase is separated
  2. 2
    Extractionthe aqueous layer is extracted with 10 mL ethyl acetate
  3. 3
    DryingThe combined organic layers are dried over sodium sulfate
  4. 4
    Concentrationconcentrated in vacuo
  5. 5
    Otherchromatographed on silica (0–1% methyl alcohol in methylene chloride)

Procedure

A mixture of 5-bromothiophene-2-sulfonamide (0.50 g, 2.1 mmol), triethyl amine (1 mL), methanol (1 mL), palladium acetate (0.046 g, 2.1 mmol) and 1,3-bis(diphenylphosphino) propane (0.085 g, 2.1 mmol) (addition in that order) in dimethylformamide (5 mL, anhydrous) is saturated with carbon monoxide gas, at room temperature. This reaction mixture is heated to 100° C. and stirred overnight, under a carbon monoxide atmosphere. 10 mL of brine and 10 mL of ethyl acetate are added to the reaction mixture. The organic phase is separated and the aqueous layer is extracted with 10 mL ethyl acetate. The combined organic layers are dried over sodium sulfate, concentrated in vacuo, and then chromatographed on silica (0–1% methyl alcohol in methylene chloride) to give the title compound, as a yellow solid (0.15 g, 34% yield).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07084170B2uspto-grants-2006_08