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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 621756Generated: October 31, 2026

Sodium borohydride → HCID 15748195, compound

https://huagongshe.com/reaction/621756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 14554062HCID 14554062—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15748195HCID 1574819589.6%

Reaction Steps

To a solution of 3,4,5,7-tetra-O-benzyl-1-deoxy-1-(dimethoxyphosphoryl)-D-gluco-2-heptulopyranose (13.8 g) in tetrahydrofuran (140 ml) was added sodium borohydride (1.4 g). The mixture was stirred overnight at room temperature. The reaction mixture was concentrated under reduced pressure, and the residue was distributed between ethyl acetate (500 ml) and water (300 ml). The ethyl acetate layer was washed with water, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The concentrate was subjected to a silica gel column chromatography (550 ml) with tolueneacetone (2:1). The elute was concentrated under reduced pressure and dried under reduced pressure to give a mixture (12.4 g) of 3,4,5,7-tetra-O-benzyl-1-deoxy-1-(dimethoxyphosphoryl)-D-glycero-D-gulo-heptitol and 1,3,4,5-tetra-O-benzyl-7-deoxy-7-(dimethoxyphosphoryl)-D-glycero-L-gulo-heptitol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04824943
Source datasetuspto-grants-1989_04
ORD IDord-56790760a7c54c55b897adcb8948181a
Source noteuspto-grants-1989_04