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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2421265Generated: November 1, 2026

4-Nitrobenzaldehyde → HCID 15516569, compound

https://huagongshe.com/reaction/2421265

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitrobenzaldehydeHCID 541—
ReactantMethanolHCID 887—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 9933557HCID 9933557—
SolventWaterHCID 962—
ProductHCID 15516569HCID 1551656955%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07956075B2
Source datasetuspto-grants-2011_06
ORD IDord-974f682a96b04de781aaa9d938f193b4
Source noteuspto-grants-2011_06