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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720049Generated: October 29, 2026

Water → HCID 21902101, compound

https://huagongshe.com/reaction/720049

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 21901928HCID 21901928—
SolventMethanolHCID 887—
ProductHCID 21902101HCID 2190210166.4%

Reaction Steps

1-(1-Benzo[1,3]dioxol-5-yl-cyclobutyl)-2-[3-(4-trifluoromethyl-phenoxymethyl)-piperidin-1-yl]-ethanone (15 mg) was dissolved in 2 mL of dry methanol and solid sodium borohydride (10 equiv.) was added in portions. Water (5 mL) was added and the mixture was extracted with ether and the ether extracts were concentrated in vacuo and purified on silica gel to give the desired 1-(1-benzo[1,3]dioxol-5-yl-cyclobutyl)-2-[3-(4-trifluoromethyl-phenoxymethyl)-piperidin-1-yl]-ethanol (10 mg, 66%). Data for this mixture of diastereomeric amino alcohols: MS 478 (M+1); 1H NMR (300 MHz, CDCl3) partial: δ 6.7–7.8 (m, 7H), 3.85–3.95 (m, 2H, methylene adjacent to aryl ether), the δ 3.1 singlet for the starting material was absent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07132551B2
Source datasetuspto-grants-2006_11
ORD IDord-3828489a4cc94a818a8a9f24a890b562
Source noteuspto-grants-2006_11