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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 130617Generated: October 26, 2026

Sodium borohydride → Di-tert-butyl cyclopropane-1,2-dicarboxylate

https://huagongshe.com/reaction/130617

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantDi-tert-butyl 1-bromocyclopropane-1,2-dicarboxylateHCID 23158974—
CatalystDichlorocobalt hexahydrateHCID 517166—
SolventDimethylacetamideHCID 31374—
ProductDi-tert-butyl cyclopropane-1,2-dicarboxylateHCID 23158971100%

Reaction Steps

Sodium borohydride (35.7 mg, 0.944 mmol) was added to and dissolved in N,N-dimethylacetamide (1.5 mL) at room temperature, followed by addition of an N,N-dimethylacetamide solution (1.0 mL) of di-tert-butyl 1-bromocyclopropane-1,2-dicarboxylate (cis/trans=11/89) (hereinafter the compound will be referred to as “compound (4c)”) (202 mg, 0.629 mmol) at 10° C. Without manipulating the temperature of the reaction, cobalt chloride hexahydrate (0.7 mg, 0.003 mmol) was added to the resultant solution. After completion of addition, the resultant mixture was stirred at 10° C. for 15 minutes. After completion of reaction, the entirety of the reaction mixture was diluted with an HPLC mobile phase to 20 mL, to thereby yield a solution containing 152.4 mg (yield: 100%) of the title compound. Yield was determined by means of high performance liquid chromatography (HPLC) (the same shall apply hereinafter).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07381833B2
Source datasetuspto-grants-2008_06
ORD IDord-9a7d51a64f7049b88b756a6634157761
Source noteuspto-grants-2008_06