Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 105601-94-3 | HCID 11095044 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 10892715 | HCID 10892715 | 97% |
Reaction Steps
A solution of 70 g (0.414 mol) (S)-2-bromo -1,4-butanediol in 1.5 liters methylene chloride was cooled in ice and 173 ml (1.24 mol) triethylamine (dried over potassium hydroxide) was added to give a clear solution. To this was added dropwise over 80 minutes at 5° to 15° C., 96 ml (1.24 mol) methanesulfonyl chloride. The mixture was then stirred at room temperature for 2.5 hours, washed 2×750 ml with water and 1×750 ml brine, dried (MgSO4), and the solvent evaporated to give an amber oil which was purified by chromatography on a 140 mm×25 cm silica gel column, eluting with 9:1 chloroform:ethyl acetate. The product fractions were combined and solvent evaporated to give 105 g (97%) of the title compound as a waxy white solid; [alpha]D=- 34.49° (c=5 in CHCl3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05191077 |
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| Source dataset | uspto-grants-1993_03 |
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| ORD ID | ord-2c08d24af0514de7a0e80e7101de17d1 |
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| Source note | uspto-grants-1993_03 |
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