HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → ethyl 2-((3aR,6R,6aR)-6-hydroxyhexahydro-furo[3,2-b]furan-3-yl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Ethyl(2E)-2-[(3R,3aS,6aR)-3-[tert-butyl(dimethyl)silyl]oxy-2,3,3a,6a-tetrahydrofuro[3,2-b]furan-6-ylidene]acetate | HCID 131735088 | — |
| Catalyst | Dichloronickel;hexahydrate | HCID 11791229 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | ethyl 2-((3aR,6R,6aR)-6-hydroxyhexahydro-furo[3,2-b]furan-3-yl)acetate | HCID 90042054 | — |
Reaction Steps
A 20 mL vessel was charged ethyl(2E)-2-[(3R,3aS,6aR)-3-[tert-butyl(dimethyl)silyl]oxy-2,3,3a,6a-tetrahydrofuro[3,2-b]furan-6-ylidene]acetate (45 mg, 0.137 mmol), nickel chloride hexahydrate (32.6 mg, 0.137 mmol) and ethanol (1 mL). Sodium borohydride (51.8 mg, 1.37 mmol) was added slowly and the mixture was stirred at room temperature for 1 h. The reaction was quenched with water (0.5 mL) and partitioned between water (4 mL) and ethyl acetate (10 mL). The aqueous layer was extracted with ethyl acetate (3×5 mL). The combined organic phases were dried over MgSO4, filtered and concentrated to afford the title compound. LC-MS: calculated for C1OH16O5, [M+Na]+Calc: 239.1. Found: 239.1, Rt=0.22 min (4 min run).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09290517B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-1e1902d9181d46e4b17863ef094c019d |
| Source note | uspto-grants-2016_03 |