Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 373255Generated: October 31, 2026

Sodium borohydride → HCID 131717632, compound

https://huagongshe.com/reaction/373255

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 131717633HCID 131717633—
SolventMethanolHCID 887—
ProductHCID 131717632HCID 131717632—

Reaction Steps

(1S,5S,6S,7R)-3-[4-Methoxycarbonyl-1(EZ)-butenyl]-6-[4,4-difluoro-3-oxo-(E )-1-octenyl]-7-tetrahydropyranyloxy-bicyclo[3.3.0]oct-2-ene (16) (0.196 g) was dissolved in methanol. To the solution, sodium borohydride (0.015 g) was added at 0° C., and the mixture was stirred for 30 minutes. After a usual work-up (1S,5S,6S,7R)-3-[4-methoxycarbonyl-1(EZ)-butenyl]-6-[4, 4-difluoro-3-(RS)hydroxy-(E)-1--octenyl]-7-tetrahydropyranyloxy-bicyclo[3.3.0]oct-2-ene (17) was obtained as a colorless oily product. Yield: 0.184 g (93%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05162370
Source datasetuspto-grants-1992_11
ORD IDord-fbd596d58e4d4ebc91f37bfbbf5a543b
Source noteuspto-grants-1992_11