HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 59381321, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 59381323 | HCID 59381323 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 59381321 | HCID 59381321 | — |
Reaction Steps
Thereafter, 500 mg of (1-pyrenyl)methyl 5-(1,2-dithiolan-3-yl)pentanoate was dissolved in DI water, 30 mg of NaBH4 was added, and the solution was stirred for 30 min at room temperature. The organic phase in the mixture solution was extracted by chloroform and dehydrated by anhydrous MgSO4, and then the organic solvent in the organic phase was removed leaving (1-pyrenyl)methyl 6,8-dimercaptooctanoate as a linking molecule. Because the 1H-NMR spectrum thereof was similar to that before the reduction reaction and the reverse reaction occurred readily, the product was not characterized but directly used to form covalent bonds with the quantum dots.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07754107B2 |
| Source dataset | uspto-grants-2010_07 |
| ORD ID | ord-80961f079063436d8148d6ab17cfe742 |
| Source note | uspto-grants-2010_07 |