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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1063370Generated: October 30, 2026

Formaldehyde → Tert-butyl 4-(3-hydroxyprop-1-yn-1-yl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1063370

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantTert-butyl 4-(2,2-dibromovinyl)piperidine-1-carboxylateHCID 11474132—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 4-(3-hydroxyprop-1-yn-1-yl)piperidine-1-carboxylateHCID 6978634586%

Reaction Steps

A solution of 6.0 g (16.3 mmol) of 4-(2,2-Dibromo-vinyl)-piperidine-1-carboxylic acid tert-butyl ester in 150 ml THF was treated at −78° C. with 21.4 ml (34.2 mmol) of n-BuLi (ca 1.6 M in hexane). After 2 h at this temperature 4.9 g (16.3 mmol) of paraformaldehyde were added. The reaction was warmed up to RT for 3 h and after 1 h at this temperature partitioned between water/ether (3×). The organic phases were washed with aqueous 10% NaCl, dried over Na2SO4 and evaporated. Purification by flash-chromatography on silica gel (hexane/EtOAc 4:1) gave 3.34 g (86%) of 4-(3-Hydroxy-prop-1-ynyl)-piperidine-1-carboxylic acid tert-butyl ester, MS: 239 (M).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06964974B2
Source datasetuspto-grants-2005_11
ORD IDord-02f7d00b87ec4b98abdc6aa25332ee64
Source noteuspto-grants-2005_11