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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2224025Generated: October 31, 2026

Water → ((3S,6R)-6-hydroxy-1-methyl-2-oxo-azepan-3-yl)-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/2224025

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant[(3S,6R)-6-(tert-butyl-dimethyl-silanyloxy)-1-methyl-2-oxo-azepan-3-yl]-carbamic acid tert-butyl esterHCID 69266856—
SolventTetrahydrofuranHCID 8028—
Product((3S,6R)-6-hydroxy-1-methyl-2-oxo-azepan-3-yl)-carbamic acid tert-butyl esterHCID 6926896196.9%

Reaction Steps

To a solution of [(3S,6R)-6-(tert-butyl-dimethyl-silanyloxy)-1-methyl-2-oxo-azepan-3-yl]-carbamic acid tert-butyl ester (0.85 g, 2.27 mmol) in THF (40 mL) is added tetrabutylammonium fluoride (3 mL 1M THF, 3 mmol) at room temperature. The reaction solution is stirred for 4 h, then H2O (40 mL) is added and the solution concentrated under vacuum to ½ its volume and extracted 3× with CH2Cl2 (40 mL). The combined CH2Cl2 extracts are adsorbed on silica and chromatographed (5% CH3OH/CH2Cl2) to give 0.568 g (72%) of ((3S,6R)-6-hydroxy-1-methyl-2-oxo-azepan-3-yl)-carbamic acid tert-butyl ester as a white solid. 1H NMR (CDCl3) δ 1.44 (s, 9H), 1.7-2.05 (m, 4H), 3.1 (s, 3H), 3.37 (dd, 1H), 3.73 (d, 1H), 4.07 (m, 1H), 4.31 (m, 1H), 6.0 (d, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07378410B2
Source datasetuspto-grants-2008_05
ORD IDord-1e0c73c7c85949d3a2153bf08db232ec
Source noteuspto-grants-2008_05