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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | tert-Butyl 2-(hydroxymethyl)morpholine-4-carboxylate | HCID 5201202 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | tert-Butyl 2-(bromomethyl)morpholine-4-carboxylate | HCID 57418765 | 37.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07799782B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-d20445ecc9fe416087d701a17e88c38a |
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| Source note | uspto-grants-2010_09 |
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