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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1852200Generated: October 31, 2026

Diisopropylethylamine → (3R)-ethyl 2-(tert-butoxycarbonylamino)-3,5-dimethylnon-8-enoate

https://huagongshe.com/reaction/1852200

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantDi-tert-butyl dicarbonateHCID 90495—
Reactant(3R)-ethyl 2-amino-3-ethyl-5-methylnon-8-enoate hydrochlorideHCID 86683258—
SolventDichloromethaneHCID 6344—
Product(3R)-ethyl 2-(tert-butoxycarbonylamino)-3,5-dimethylnon-8-enoateHCID 8668323562.5%

Reaction Steps

A solution of (3R)-ethyl 2-amino-3-ethyl-5-methylnon-8-enoate hydrochloride (2.99 g, 10.77 mmole) in DCM (20 mL) was added DIPEA (1.08 mL, 10.77 mmole) followed by (BOC)2O (2.39 mL, 10.77 mmole) at room temperature. The reaction mass was stirred at room temperature for overnight. The reaction mass was diluted with DCM and washed with water. The organic layer was dried over anhydrous Na2SO4 and evaporated under reduced pressure to get crude compound. The crude compound was purified by column chromotography (Silica gel, 20% ethyl acetate in pet-ether) to get 2.3 g, (62.5%) of (3R)-ethyl 2-(tert-butoxycarbonylamino)-3,5-dimethylnon-8-enoate as an oily liquid. MS: MS m/z 342.4 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957203B2
Source datasetuspto-grants-2015_02
ORD IDord-d9771bda81c743d494ff75a4061f774e
Source noteuspto-grants-2015_02