HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010541Generated: October 30, 2026
2-Chlorobenzaldehyde → HCID 86652007, compound
https://huagongshe.com/reaction/1010541
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chlorobenzaldehyde | HCID 6996 | — |
| Reactant | Sulfuric acid magnesium salt (1:1) | HCID 24083 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 86652006 | HCID 86652006 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 86652007 | HCID 86652007 | 59% |
Reaction Steps
With stirring and cooling in an ice-water bath (0° C.) 0.12 grams (0.0004 mole) of [(6-chloro(3-pyridyl))methyl]{2-[2-(nitromethylene)imidazolidinyl]ethyl]amine, 0.06 gram (0.0004 mole) of 2-chlorobenzaldehyde, 0.13 gram (0.0006 mole) of sodium triacetoxyborohydride and 0.10 gram (0.0008 mole) of magnesium sulfate in about 20 mL of 1,2-dichloroethane were combined. Upon completion of addition, the cooling bath was removed and the reaction mixture was allowed to warm to ambient temperature as it stirred during an 18 hour period. After this time the reaction was quenched by the addition of five mL of water, then the reaction mixture was neutralized to pH of 8-9. The reaction mixture was then extracted with two 50 mL portions of methylene chloride. The combined extracts were dried with sodium sulfate, filtered and concentrated under reduced pressure, yielding 0.07 gram of Compound 501. The
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07977332B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-ef9794a0c4b7466ea036db344c5f5eaa |
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| Source note | uspto-grants-2011_07 |
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