Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2-Carboxymethylthio-2-methyltetrahydrofuran | HCID 19957989 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19920480 | HCID 19920480 | — |
Reaction Steps
To a solution of 2 mmol of 26 in 10 mL of anhydrous tetrahydrofuran (kept at 0° C.) 3 mL of BH3. THF complex (lM) is added slowly. The mixture is stirred for 3 hours in a nitrogen atmosphere at 0° C. Approximately 10 mL of water added slowly and the reaction is stirred for 15 min. The mixture is concentrated in vacuo at 40°-45° C. and the aqueous residue is extracted with ethyl acetate. The organic layer is washed with 10% bicarbonate. The ethyl acetate layer is dried and evaporated to give the product, 27 as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04988496 |
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| Source dataset | uspto-grants-1991_01 |
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| ORD ID | ord-845f24befaec40de84d45351e0cf123a |
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| Source note | uspto-grants-1991_01 |
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