Diethyl Ether → 2-[(2-phenylethanethioyl)sulfanyl]propanoic Acid

A solution of benzylmagnesium chloride in ether (1.0 M, 40 mL, 40 mmol) was added slowly with stirring to an ice-cooled solution of carbon disulfide (4.0 mL, 66 mmol) in dry tetrahydrofuran (40 mL) under nitrogen. After 30 min, 2-bromopropanoic acid (3.6 mL, 6.2 g, 40 mmol) was added and the reaction was stirred at ambient temperature. After 48 h, the mixture was poured into ethyl acetate (200 mL) and washed with water (3×100 mL), followed by saturated sodium chloride solution (100 mL). The organic layer was dried (magnesium sulfate) and evaporated. The remaining liquid was distilled (120°/0.13 Pa, Kugelrohr) to remove unreacted 2-bromopropanoic acid. The residue was then dissolved in ether (200 mL) and extracted with 5% sodium bicarbonate solution (4×50 mL). The combined aqueous extracts were washed with ether (100 mL), then acidified to pH<1 with 2 M hydrochloric acid. The resulting mixture was extracted with ethyl acetate (2×100 mL) and the combined organic extracts were washed with water (2×50 mL), saturated sodium chloride (50 mL) and then dried with magnesium sulfate. Evaporation of the solvent gave the title compound (20) as a red liquid (3.73 g, 39%) which slowly solidified on standing.

1. waitAfter 48 h
2. washwashed with water (3×100 mL)
3. dry with materialThe organic layer was dried (magnesium sulfate)
4. customevaporated
5. distillationThe remaining liquid was distilled (120°/0.13 Pa, Kugelrohr)
6. customto remove unreacted 2-bromopropanoic acid
7. dissolutionThe residue was then dissolved in ether (200 mL)
8. extractionextracted with 5% sodium bicarbonate solution (4×50 mL)
9. washThe combined aqueous extracts were washed with ether (100 mL)
10. extractionThe resulting mixture was extracted with ethyl acetate (2×100 mL)
11. washthe combined organic extracts were washed with water (2×50 mL), saturated sodium chloride (50 mL)
12. dry with materialdried with magnesium sulfate
13. customEvaporation of the solvent

ORD record

ord-589f65e42641419ab062bba18270b031

Source dataset

uspto-grants-2010_06

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07745553B2