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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349247Generated: October 26, 2026

2-Methoxy-5-(trifluoromethoxy)benzaldehyde → 2-Methoxy-5-(trifluoromethoxy)benzyl alcohol

https://huagongshe.com/reaction/349247

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methoxy-5-(trifluoromethoxy)benzaldehydeHCID 2783364—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product2-Methoxy-5-(trifluoromethoxy)benzyl alcoholHCID 501124675.5%

Reaction Steps

Dissolve 2-methoxy-5-trifluoromethoxy-benzaldehyde (9.0 g, 40.9 mmol) in MeOH (100 mL) and treat with sodium borohydride (1.45 g, 38.3 mmol). Stir at RT for 1 h., then carefully quench with 1N HCl to pH 3. Concentrate, then extract the aqueous mixture with CH2Cl2 (3×100 mL). Combine the organic phases and wash with saturated NaHCO3 (100 mL) and brine (100 mL). Dry the organic layer, then filter, and concentrate. Purify the crude material by flash chromatography using a linear gradient of 100% hexanes to 40% EtOAc/hexanes to give (2-methoxy-5-trifluoromethoxy-phenyl)-methanol (6.86 g, 75%) as a colorless oil. 1H NMR (400 MHz, CDCl3) δ 7.19 (m, 1H), 7.10 (dd, 1H, J=2.9, 8.8 Hz), 6.83 (d, 1H, J=8.8 Hz), 4.66 (d, 2H, J=6.4 Hz), 3.85 (s, 3H), 2.21 (t, 1H, J=6.4 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179804B2
Source datasetuspto-grants-2007_02
ORD IDord-4896a6c2c8074929a1b7a454347ed2d5
Source noteuspto-grants-2007_02