HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 621756Generated: October 31, 2026
Sodium borohydride → HCID 15748195, compound
https://huagongshe.com/reaction/621756
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 14554062 | HCID 14554062 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 15748195 | HCID 15748195 | 89.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04824943 |
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| Source dataset | uspto-grants-1989_04 |
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| ORD ID | ord-56790760a7c54c55b897adcb8948181a |
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| Source note | uspto-grants-1989_04 |
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