HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 864996Generated: November 1, 2026
Water → (-)-2-(2-Amino-6-chloropurin-9-ylmethyl)-1,4-butanediol
https://huagongshe.com/reaction/864996
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | Dimethyl 2-(2-amino-6-chloropurin-9-ylmethyl)succinate | HCID 19027590 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | (-)-2-(2-Amino-6-chloropurin-9-ylmethyl)-1,4-butanediol | HCID 19027588 | 100% |
Reaction Steps
To a solution of (-)-dimethyl-2-(2-amino-6-chloropurin-9-ylmethyl)succinate (enantiomeric excess 85%; 19.9 mg, 0.0607 mmol), dissolved in tert. butanol (2.0 ml) at 40° C., was added lithium borohydride (30 mg, 1.38 mmol) in portions with stirring After 1 h at ambient temperature, water (0.3 ml) was added slowly and stirring continued over night. Inorganic salts were filtered, washed carefully with tert. butanol and the solution was evaporated to dryness. Preparative thin-layer chromatography (PSC-Fertigplatten, Merck) with chloroform+methanol (5+1) as mobile phase afforded 16.5 mg (theoretical yield) of (-)-2-(2-amino-6-chloropurin-9-ylmethyl)-1,4-butanediol. [α]D20 ° -5.20°, [α]54620 -5.92° (c 0.625, ethanol). TLC on silica (chloroform+methanol 5+1): Rf 0.40, identical to that of the racemate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05565461 |
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| Source dataset | uspto-grants-1996_10 |
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| ORD ID | ord-81a85e290ed74a21adbd898cea44a784 |
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| Source note | uspto-grants-1996_10 |
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