HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1944149Generated: October 31, 2026
Sodium borohydride → HCID 59563691, compound
https://huagongshe.com/reaction/1944149
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 59563706 | HCID 59563706 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59563691 | HCID 59563691 | — |
Reaction Steps
To a suspension of CoCl2.6H2O in THF was added ethyl 2-cyano-2-(4-((triisopropylsilyloxy)methyl)phenyl)acetate (E200). The mixture was cooled to 0° C. and NaBH4 was added to the mixture in several portions over 30 min. The mixture was stirred at room temperature for 4 h. The reaction was quenched with water. The mixture was filtered and the filtrate extracted twice with ether. The organics were dried (MgSO4), filtered, and evaporated. Column chromatography (SiO2, DCM:EtOH=50:1) gave pure ethyl 3-amino-2-(4-((triisopropylsilyloxy)methyl)phenyl)propanoate (E201) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08394826B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-0b44c41ec18e4e4f86298d1e2b2de6aa |
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| Source note | uspto-grants-2013_03 |
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