Diiodomethane → Methyl 4-[(acetylsulfanyl)methyl]oxane-4-carboxylate

n-Butyllithium (49.8 ml of a 1.6 N solution in hexanes) was added gradually to a solution of diisopropylamine (11.2 ml) in tetrahydrofuran (90 ml) cooled in an acetone-cardice bath under an atmosphere of nitrogen. After stirring for 30 minutes, ethyl cyclobutanecarboxylate (10 ml) was added. The mixture was stirred for a further 30 minutes before addition of diiodomethane (6.4 ml), and then for 3 hours, during which it warmed to room temperature. It was quenched with water (30 ml) and the tetrahydrofuran. evaporated in vacuo. The residue was partitioned between ethyl acetate (100 ml) and water (100 ml). The aqueous was extracted with ethyl acetate (100 ml). The combined organics were dried (MgSO4) and the solvent removed in vacuo to give a brown oil which was dissolved in N,N-dimethylformamide (40 ml) and added to a suspension of potassium thioacetate (8.3 g) in N,N-dimethylformamide (40 ml) at room temperature. The mixture was stirred for 18 hours before evaporation of the solvent in vacuo. The residue was partitioned between ethyl acetate (100 ml) and water (100 ml). The organics were washed with water (100 ml), dried (MgSO4) and the solvent removed in vacuo to give the title compound (13.5 g) as a brown oil.

1. temperaturecooled in an acetone-cardice bath under an atmosphere of nitrogen
2. waitfor 3 hours
3. customIt was quenched with water (30 ml)
4. customevaporated in vacuo
5. customThe residue was partitioned between ethyl acetate (100 ml) and water (100 ml)
6. extractionThe aqueous was extracted with ethyl acetate (100 ml)
7. dry with materialThe combined organics were dried (MgSO4)
8. customthe solvent removed in vacuo
9. customto give a brown oil which
10. stirringThe mixture was stirred for 18 hours before evaporation of the solvent in vacuo
11. customThe residue was partitioned between ethyl acetate (100 ml) and water (100 ml)
12. washThe organics were washed with water (100 ml)
13. dry with materialdried (MgSO4)
14. customthe solvent removed in vacuo

ORD record

ord-ab0cdf92a3a04c1f9b45bcc8d3ab05d7

Source dataset

uspto-grants-2004_01

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US06680338B2