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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504834Generated: October 31, 2026

Hydrazine hydrate (1:1) → tert-butyl N-[1-amino-3-(methylsulfanyl)propan-2-yl]carbamate

https://huagongshe.com/reaction/1504834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactanttert-Butyl [2-phthalimido-1-(methylsulfanylmethyl)ethyl]carbamateHCID 24720892—
SolventEthanolHCID 702—
Producttert-butyl N-[1-amino-3-(methylsulfanyl)propan-2-yl]carbamateHCID 72455593—

Reaction Steps

To a solution of tert-butyl [1-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-3-(methylsulfanyl)propan-2-yl]carbamate (from Step 3 of PrepEx 4.11) (10.0 g, 28.6 mmol) in ethanol (150 mL) was added dropwise hydrazine hydrate (15.7 g, 286 mmol) at 0° C. and then the reaction mixture was allowed to warm to ambient temperature. After 30 minutes, the reaction mixture was heated to reflux. After two hours, the reaction mixture was cooled, filtered, and concentrated under reduced pressure. The residue was purified by chromatography on silica gel to give tert-butyl [1-amino-3-(methylsulfanyl)propan-2-yl]carbamate. MS ESI calc'd. for C9H21N2O2S [M+H]+ 221. found 221. 1H NMR (400 MHz, CD3OD) δ 3.66-3.63 (m, 1H), 2.83-2.79 (m, 1H), 2.64-2.50 (m, 3H), 2.12 (s, 3H), 1.45 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216173B2
Source datasetuspto-grants-2015_12
ORD IDord-b40620f37a934282a7b5552bd37843b5
Source noteuspto-grants-2015_12