HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1787842Generated: October 31, 2026
Sodium borohydride → HCID 68877648, compound
https://huagongshe.com/reaction/1787842
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Calcium Chloride | HCID 5284359 | — |
| Reactant | HCID 68877168 | HCID 68877168 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68877648 | HCID 68877648 | — |
Reaction Steps
13 g of methyl 2-benzyloxy-5-(1-hydroxy-2-{3-[3-(4-methoxy-phenyl)-imidazol-1-yl]-1,1-dimethyl-propylamino}-ethyl)-benzoate in 100 mL tetrahydrofuran are reacted with a solution of 6.5 g of calcium chloride in 65 mL ethanol and 4.5 g of sodium borohydride analogously to the method used for Example 1c. After a reaction time of 12 hours, 3 g of calcium chloride, dissolved in 30 mL ethanol, and 2 g of sodium borohydride are added and stirring is continued for a further 12 hours. Then the mixture is worked up as described, except that extraction is carried out using chloroform rather than ethyl acetate. During the evaporation of this organic phase a solid is precipitated out. The solid is suction filtered, stirred with ethyl acetate and recrystallised from acetonitrile. Yield: 79.5 g (77%); m.p.=108-111° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07511067B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-0b6542bca0fa4b02977893324d8e1da7 |
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| Source note | uspto-grants-2009_03 |
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