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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 929163Generated: November 2, 2026

Sodium borohydride → ethyl 2-((3aR,6R,6aR)-6-hydroxyhexahydro-furo[3,2-b]furan-3-yl)acetate

https://huagongshe.com/reaction/929163

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantEthyl(2E)-2-[(3R,3aS,6aR)-3-[tert-butyl(dimethyl)silyl]oxy-2,3,3a,6a-tetrahydrofuro[3,2-b]furan-6-ylidene]acetateHCID 131735088—
CatalystDichloronickel;hexahydrateHCID 11791229—
SolventEthanolHCID 702—
Productethyl 2-((3aR,6R,6aR)-6-hydroxyhexahydro-furo[3,2-b]furan-3-yl)acetateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290517B2
Source datasetuspto-grants-2016_03
ORD IDord-1e1902d9181d46e4b17863ef094c019d
Source noteuspto-grants-2016_03