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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 68217Generated: October 25, 2026

Sodium Thiosulfate → tert-Butyl N-(3-oxopropyl)carbamate

https://huagongshe.com/reaction/68217

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantTriacetoxyperiodinaneHCID 159087—
Reactanttert-butyl N-(3-hydroxypropyl)carbamateHCID 3838134—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventSodium BicarbonateHCID 516892—
Producttert-Butyl N-(3-oxopropyl)carbamateHCID 1091005186.8%

Reaction Steps

To a stirring solution of 3-(Boc-amino)-1-propanol (25 mL, 0.144 mol) in water saturated DCM (1.0 L) was added Dess-Martin reagent (99.2 g, 233.9 mmol) and the reaction mixture was stirred for 1 hour. The reaction was then diluted with ether (1.0 L), followed by a solution of Na2S2O3 (250 g) in 80% NaHCO3 (450 g in 1.0 L H2O). The reaction was stirred vigorously for 30 minutes until two layers formed, the top layer was clear. The reaction was filtered to remove the precipitated solids and the aqueous layer was extracted with ether (1.0 L). The organic layer was washed with sat. NaHCO3 (1.0 L), H2O (1.0 L), and brine (1 L), dried over Na2SO4 and concentrated to a clear oil. The crude oil was dissolved in EtOAc:hexanes (1:1 v/v, 1.0 L) and filtered through a short silica gel column to yield the desired N-Boc-3-amino-propanal (21.7 g, 0.125 mol, 85.6% yield): 1H NMR (400 MHz, CDCl3) δ 9.77 (s, 1H, CHO), 4.85 (bs, 1H, NH), 3.36-3.42 (m, 2H, CH2), 2.67 (t, 2H, CH2), 1.39 (s, 9H, (CH3)3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822424B2
Source datasetuspto-grants-2014_09
ORD IDord-ed7443ca222e4edfb54296bd8b988bc4
Source noteuspto-grants-2014_09