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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1492023Generated: October 31, 2026

HCID 18657616, compound → HCID 44305824, compound

https://huagongshe.com/reaction/1492023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 18657616HCID 18657616—
ReactantHCID 67797893HCID 67797893—
SolventMethanolHCID 887—
ProductHCID 44305824HCID 44305824—

Reaction Steps

(Z)-(2R,3R,4S)-7-[4-(biphenyl-4-ylmethoxy)-2-(3-pyridyl)tetrahydrofuran-3-yl]hept-4-enoic acid having mp 94°-96° C. and [α]D25 =-83.75° (MeOH) is prepared from (2R,3R,4S)-3-(3-t-butyldimethylsilyloxypropan-1-yl)-4-[(R)-(-)-α-methoxyphenylacetoxy]-2-(3-pyridyl)tetrahydrofuran as described for the synthesis of (Z)-(2S,3S,4R)-7-[4-(biphenyl-4-ylmethoxy)-2-(3-pyridyl)tetrahydrofuran-3-yl]hept-4-enoic acid in example 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05371096
Source datasetuspto-grants-1994_12
ORD IDord-c9963b0a3fb64407a54ea0ac242228f4
Source noteuspto-grants-1994_12