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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 966864Generated: October 30, 2026

Methanol → [5-(Butylsulfanyl)thiophen-2-yl]methanol

https://huagongshe.com/reaction/966864

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86588308HCID 86588308—
SolventTetrahydrofuranHCID 8028—
SolventSodium HydroxideHCID 14798—
Product[5-(Butylsulfanyl)thiophen-2-yl]methanolHCID 22292447—

Reaction Steps

A solution of NaBH4 (5.3 g, 0.141 mol) in methanol (29.0 g) and sodium hydroxide (20%, 56.0 mL) was added dropwise to a solution of 45 (56.47 g, 0.282 mol) in THF (75 mL) at room temperature. The mixture was stirred for 2 hours, extracted with ethyl ether 3×150 mL), the combined extracts washed with brine and dried (MgSO4). After solvent removal, the crude product 46 was obtained as an oil (55.4 g, 97%); 1H NMR δ: 0.88 (t, 3 H, J=7.3 Hz, CH3), 1.39 (m, 2 H, CH3—CH2), 1.57 (m, 2 H, CH3—CH2—CH2),1.88 (s, 1 H OH), 2.76 (t, 2 H, J=7.3 Hz, CH2—S), 4.73 (s, 2 H, CH2—OH), 6.83 (d, 1 H, J=3.5 Hz, aromatic H), 6.94 (d, 1 H, J=3.5 Hz, aromatic H); λmax/nm (εmax/dm3 mol−1cm−1) 275.5 (3600); LRMS(EI+) calc. for C9H14OS2: 202.1, found 202.1. The product was used without further purification in the preparation of 47.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06953570B2
Source datasetuspto-grants-2005_10
ORD IDord-39088f566e7c48dc9ce43205bf4571ef
Source noteuspto-grants-2005_10