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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1196694Generated: November 1, 2026

Sodium borohydride → HCID 15078286, compound

https://huagongshe.com/reaction/1196694

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 10008259HCID 10008259—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 15078286HCID 15078286—

Reaction Steps

35 g of (-)-(1S)-1-(3-methylsulfonyl-4-n-propoxy-5-benzyloxyphenyl)-4-(3,4,5-trimethoxyphenyl) butan-1-ol-4-one (STEP E) dissolved in a mixture of 300 mL dry THF and 100 mL of methanol was treated with 3.5 g of NaBH4 at 0° C. and stirred for 3 h. The reaction mixture was then allowed to gradually warm to room temperature and stirring was continued for additional 2 h. After the completion of the reaction, the solvent was evaporated at reduced pressure and the residue obtained as such was redissolved in 300 ml of ethyl acetate. The organic layer was washed with 1.5N HCl, distilled water and brine respectively, and then dried over MgSO4 and evaporated to yield a colorless syrup which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05114961
Source datasetuspto-grants-1992_05
ORD IDord-7df0d47f2a084c278e62a044dd735c01
Source noteuspto-grants-1992_05