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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1741440Generated: October 31, 2026

Triethylamine → HCID 21835840, compound

https://huagongshe.com/reaction/1741440

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1,3-PropanediolHCID 10442—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 21835824HCID 21835824—
SolventIsopropanolHCID 3776—
ProductHCID 21835840HCID 2183584075%

Reaction Steps

2.29 g (11.2 mmol) of 2-(3,4-dimethylbenzyloxy)ethylazide obtained in step 2 was dissolved in 15 ml of isopropanol while stirring, and 3.1 ml (22 mmol) of triethylamine was added thereto. The mixture was added to an isopropanol solution containing 1.1 ml (11 mmol) of 1,3-propanediol and then 4.22 g (0.11 moles) of NaBH4 was added thereto. The mixture was stirred at an ambient temperature for 1 hour and the solvent was distilled off under a reduced pressure. The residue was dissolved in 10% aqueous citric acid and the resulting solution was washed three times with 30 ml of ether: hexane (1:1). The pH of the aqueous layer was adjusted to 12 with a 6N sodium hydroxide solution and then a saturated sodium chloride solution was added thereto. Thee aqueous layer was extracted with 30 ml of dichloromethane 3 times. The organic layer was dried and the solvent was evaporated under a reduced pressure to obtain 1.49 g (yield 75%) of the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05973201
Source datasetuspto-grants-1999_10
ORD IDord-07e453694b6e42079f43a77718d14af3
Source noteuspto-grants-1999_10