Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 928001Generated: November 3, 2026

Sodium borohydride → HCID 86713328, compound

https://huagongshe.com/reaction/928001

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86713329HCID 86713329—
SolventEthanolHCID 702—
ProductHCID 86713328HCID 8671332854.7%

Reaction Steps

Sodium borohydride (0.32 g) was added in portions to a stirred solution of tert-butyl (1aRS,7bSR)-5-(trifluoroacetylamino)-1,1a,2,7b-tetrahydro-cyclopropa-[c]chromene-4-carboxylate (Intermediate 123, 0.5 g) in ethanol (20 mL). The resultant mixture was stirred at room temperature for 1 hour then concentrated under vacuum. The residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and petroleum ether with a gradient of 2-4% to give tert-butyl (1aRS,7bSR)-5-amino-1,1a,2,7b-tetrahydrocyclopropa-[c]chromene-4-carboxylate (0.2 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290472B2
Source datasetuspto-grants-2016_03
ORD IDord-d6d62857031941e78a8fb016a6b488c7
Source noteuspto-grants-2016_03