HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591770Generated: October 30, 2026
4-Nitrobenzaldehyde → HCID 15516569, compound
https://huagongshe.com/reaction/1591770
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Nitrobenzaldehyde | HCID 541 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 9933557 | HCID 9933557 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 15516569 | HCID 15516569 | 55% |
Reaction Steps
0.5 g (1.57 mmol) of the compound of Example 9, 0.237 g (1.57 mmol) of 4-nitrobenzaldehyde and 1 g of previously activated pulverulent 4 Å molecular sieve are added successively to a flask containing 30 ml of anhydrous MeOH, under an inert atmosphere. The reaction mixture is vigorously stirred for 18 hours before the addition, by portions, of 0.06 g (1.57 mmol) of NaBH4. Stirring is maintained for another 4 hours before the addition of 5 ml of water. After a quarter of hour, the sieve is filtered out and the reaction mixture is extracted with two times 100 ml of CH2Cl2. The organic phase is washed successively with 50 ml of water then with 50 ml of salt water, dried over sodium sulphate, filtered and concentrated under vacuum. The residue is purified on a silica column (eluent: 50% ethyl acetate in heptane). A yellow oil is obtained with a yield of 55%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07291641B2 |
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| Source dataset | uspto-grants-2007_11 |
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| ORD ID | ord-b52697feb5dc45aa84759365765f97b4 |
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| Source note | uspto-grants-2007_11 |
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