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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2085624Generated: November 2, 2026

Methanol → (R)-(-)-2-(1-n-Butoxyethoxy)-1-propanol

https://huagongshe.com/reaction/2085624

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 12994197HCID 12994197—
SolventTolueneHCID 1140—
Product(R)-(-)-2-(1-n-Butoxyethoxy)-1-propanolHCID 1299419591.4%

Reaction Steps

8.4 g (0.204 mole) of sodium borohydride was suspended at room temperature in a solution of 44.1 g (0.17 mole) of the isobutyl (R)-(+)-2-(1-n-butoxyethoxy)propionate (obtained in Reference Example 6) dissolved in 170 ml of toluene. Thereto was dropwise added slowly 41.3 ml (1.02 mole) of methanol with stirring, so that the internal temperature of the reaction system could be kept at 40° C. After the completion of the dropwise addition, the resulting mixture was stirred at room temperature for 5 hours to give rise to a reaction. To the reaction mixture was added 50 ml of water, followed by stirring for 0.5 hour. The organic layer was separated. The water layer was subjected to extraction with 50 ml of toluene. The two organic layers were combined and washed with 50 ml of water and 50 ml of a saturated aqueous sodium chloride solution in this order. The washed solution was dried over anhydrous sodium sulfate and then subjected to vacuum distillation to remove the solvent, whereby was obtained 27.4 g (yield: 91.3%) of an oily title compound (diastereomixture).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06720463B1
Source datasetuspto-grants-2004_04
ORD IDord-59e67d7df2b24cc1ac79fbadb2adb5b2
Source noteuspto-grants-2004_04