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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171014Generated: October 30, 2026

Sodium borohydride → HCID 86603464, compound

https://huagongshe.com/reaction/1171014

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86603463HCID 86603463—
SolventWater ethanolHCID 19096565—
ProductHCID 86603464HCID 86603464—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of methyl 2,4-dimethyl-6-hydroxy-3-(4′-methoxymethoxy-3′-iso-propylbenzyl)benzoate in ethanol-water (3.0 mL, 95:5) at room temperature was added NaBH4. The reaction mixture was heated at 80° C. for 4 h and cooled to room temperature. The reaction mixture was quenched with aqueous NH4Cl and extracted with ether. The organic layer was dried over MgSO4, filtered and concentrated under reduced pressure. The crude product was purified by column chromatography on silica gel, eluting with 30% acetone in hexanes to afford 2,4-dimethyl-6-hydroxy-3-(4′-methoxymethoxy-3′-iso-propylbenzyl)benzyl alcohol: 1H NMR (300 MHz, CD3OD): δ 6.97 (d, J=2.4 Hz, 1 H), 6.92 (d, J=13.2 Hz, 1 H), 6.68 (dd, J=13.2, 2.4 Hz, 1 H), 6.59 (s, 1 H), 5.17 (s, 2 H), 4.78 (s, 2 H), 3.96 (s, 2 H), 3.47 (s, 3 H), 3.30 (m, 1 H), 2.24 (s, 3 H), 2.19 (s, 3 H), 1.18 (d, J=10.8 Hz, 6 H); TLC conditions: Uniplate silica gel, 250 microns; Mobile phase=acetone-hexanes (3:7); Rf=0.40.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829552B2
Source datasetuspto-grants-2010_11
ORD IDord-9f08ed62f3e04632a01f44b0fb9db20b
Source noteuspto-grants-2010_11