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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1695928Generated: November 1, 2026

Water → (2-(2-(Piperidin-1-yl)ethylamino)-3-fluorophenyl)methanol

https://huagongshe.com/reaction/1695928

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium FluorideHCID 5235—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantMethyl 2-(2-(piperidin-1-yl)ethylamino)-3-fluorobenzoateHCID 57774462—
SolventDiethyl EtherHCID 3283—
Product(2-(2-(Piperidin-1-yl)ethylamino)-3-fluorophenyl)methanolHCID 577744026,799.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of methyl 2-(2-(piperidin-1-yl)ethylamino)-3-fluorobenzoate (740 mg, 2.640 mmol) in Et2O (30 mL) at −20° C. was treated with LAH (128 mg, 3.372 mmol). After 1.5 hours additional LAH (20 mg, 0.5269 mmol) was added and the reaction was warmed to 0° C. At 0° C., the reaction was diluted with Et2O (80 mL), then NaF and water were added with vigorous stirring until a white ppt formed and the solution cleared. The solution was decanted and evaporated under vacuum. The crude material was purified on a 12 g Redisep ISCO column with 0-10% MeOH in CH2Cl2 over 40 CV to yield (2-(2-(piperidin-1-yl)ethylamino)-3-fluorophenyl)methanol (453 mg, 179.5 mmol) as an off-white solid. FIA: 253.19 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163737B2
Source datasetuspto-grants-2012_04
ORD IDord-6dea3352313440bdbc218d029695ede3
Source noteuspto-grants-2012_04