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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 623776Generated: October 29, 2026

Sodium borohydride → HCID 86711862, compound

https://huagongshe.com/reaction/623776

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86711861HCID 86711861—
SolventMethanolHCID 887—
ProductHCID 86711862HCID 8671186250.8%

Reaction Steps

To a stirred solution of SC-187 (31 mg, 0.276 mmol) in dry MeOH (3 mL) was added CoCl2 (54 4, 1.382 mmol) under an inert atmosphere. NaBH4 (199 mg, 5.25 mmol) was added in three equal portions under a nitrogen atmosphere at −5° C. The grey reaction mixture was stirred at room temperature during 30 min. and quenched with ice (20 mL) and aqueous 0.5 M KHSO4 (20 mL). DCM (10 mL) was added and both layers were filtered over Celite. The aqueous layer was extracted twice with DCM (10 mL). The combined organic layers were washed with brine (20 mL), dried (Na2SO4), filtered and concentrated in vacuo. Purification was performed by flash chromatography (silica, CH2Cl2/MeOH, 9:1). The appropriate fractions were combined and solvents removed in vacuo. This product was combined with the crude batch from a previous experiment performed under the same reaction conditions. In this previous experiment SC-187 (14 mg, 0.023 mmol, purity: 76%), MeOH (1 mL), CoCl2 (5.72 μL, 0.148 mmol) and NaBH4 (21.2 mg, 0.561 mmol) were used. Further purification was performed by flash chromatography (silica, DCM/MeOH/Et3N, 9:1:0.1). The appropriate fractions were combined and solvents removed in vacuo. Concentration in vacuo gave SC-188 (67 mg, 46%) as a green oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09302988B2
Source datasetuspto-grants-2016_04
ORD IDord-57181139bf39408091777a15dce62d7a
Source noteuspto-grants-2016_04