Water → N-(2-Hydroxyethylamino)-ethanesulfonic acid
Reaction equation
[S:1](=[O:3])=[O:2].[N:4]1([CH2:7][CH2:8][OH:9])[CH2:6][CH2:5]1.[OH2:10]>>[OH:9][CH2:8][CH2:7][NH:4][CH2:5][CH2:6][S:1]([OH:10])(=[O:3])=[O:2]Participants
4
Conditions
- Temperature
- 10 °C
Procedure
N-(β-hydroxyethyl)-2-aminoethanesulfonic acid, ##STR7## was prepared as follows: 2250 parts water was saturated with sulfur dioxide at 10° C. in a three-necked, round-bottom flask which was fitted with an electrical stirrer, thermometer, dropping funnel, and a gas inlet tube, 261 parts 1-aziridine-ethanol dissolved in 750 parts water was added via the dropping funnel while sulfur dioxide was bubbled into the flask and the temperature maintained at 10° C. After the addition was completed, the contents of the flask were concentrated to 600 parts and added to 3000 parts ethanol (F-30). The resulting solid was washed with 2000 parts ethanol, filtered, and dried to give 340 parts of the desired product.
Workup
- customwas fitted with an electrical stirrer
- customwas bubbled into the flask
- additionAfter the addition
- concentrationthe contents of the flask were concentrated to 600 parts
- additionadded to 3000 parts ethanol (F-30)
- washThe resulting solid was washed with 2000 parts ethanol
- filtrationfiltered
- customdried
Sources & evidence
- ORD record
- ord-8b1dd2dab67b4f09bbdd705fdb1075a9
- Source dataset
- uspto-grants-1977_06
- Patent number
- US04029638
Reaction notes
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