Methanesulfonyl chloride → N-(3-bromopropyl)methanesulfonamide

To a cooled solution of 2-bromopropylamine hydrobromide (43.8 g., 0.20 mole) in pyridine (100 ml.) was added over a period of 40 minutes methanesulfonyl chloride (15.2 ml., 0.20 mole). The reaction mixture was stirred for 15 minutes and then diluted with ether. The remaining solid was filtered off, washed with about 200 ml. of acetone. The filtrate and washes were concentrated in vacuo. The residue was extracted with three 100 ml. portions of acetone. Upon evaporation of the acetone, 30.4 g. of a thick oil representing the title compound. The product was confirmed by infrared analysis and nuclear magnetic resonance.

1. filtrationThe remaining solid was filtered off
2. washwashed with about 200 ml
3. concentrationThe filtrate and washes were concentrated in vacuo
4. extractionThe residue was extracted with three 100 ml
5. customUpon evaporation of the acetone, 30.4 g

ORD-Eintrag

ord-6600b6c0234a480cb65c983a54d1d7ca

Quelldatensatz

uspto-grants-1978_01

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US04071351