Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1064861Generated: November 2, 2026

Sodium borohydride → HCID 22272611, compound

https://huagongshe.com/reaction/1064861

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 22272615HCID 22272615—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 22272611HCID 2227261198%

Reaction Steps

To a mixed solution of this aldehyde (745 mg, 3.63 mmol) in dichloromethane (5 ml) and methanol (10 ml) was added sodium borohydride (280 mg, 7.40 mmol) with ice-cooling and stirred at room temperature for 1 hour. The reaction solution was diluted with water and extracted with chloroform. The organic layer was washed with a saturated sodium hydrochloride solution, dried over anhydrous sodium sulfate and concentrated in vacuo. The resulting residue was purified by a silica gel column chromatography (silica gel 50 g, developing solvent; hexane:ethyl acetate=6:1 2:1) to provide 736 mg (yield 98%) of 4-amino-3,5-diisopropylbenzenemethanol as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06969711B2
Source datasetuspto-grants-2005_11
ORD IDord-6a7d859b8c1e48b395c89f27c20faed5
Source noteuspto-grants-2005_11