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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1715614Generated: October 25, 2026

Carbon tetrabromide → tert-Butyl 2-(bromomethyl)morpholine-4-carboxylate

https://huagongshe.com/reaction/1715614

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
Reactanttert-Butyl 2-(hydroxymethyl)morpholine-4-carboxylateHCID 5201202—
SolventDichloromethaneHCID 6344—
Producttert-Butyl 2-(bromomethyl)morpholine-4-carboxylateHCID 5741876537.3%

Reaction Steps

To a cooled (0° C.) solution of 2-hydroxymethylmorpholine-4-carboxylic acid tert-butyl ester (1.04 g, 4.79 mmol, see Step 1) in dichloromethane (20 mL) was added CBr4 (1.98 g, 5.98 mmol). After stirring the mixture for 10 minutes, triphenylphosphine (2.20 g, 8.38 mmol) was added portion-wise. The reaction mixture was stirred at 0° C. for 6 hours and then allowed to warm to room temperature and stirred for 60 hours. The mixture was concentrated under reduced pressure and then diluted with ether. The crude mixture was filtered and the filtrate was concentrated to afford the crude product, which was chromatographed on Biotage eluting with dichloromethane. The desired fractions were combined and concentrated to yield 0.50 g of product (37% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799782B2
Source datasetuspto-grants-2010_09
ORD IDord-d20445ecc9fe416087d701a17e88c38a
Source noteuspto-grants-2010_09