Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorosulfamic acid | HCID 24499 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Methyl-2-propylpropane-1,3-diol | HCID 66220 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 60548-64-3 | HCID 12708925 | — |
Reaction Steps
To a solution of 10 g. (0.076 mol.) of 2-methyl-2-propyl-1,3-propanediol in 200 ml. of dimethoxyethane is added 12.7 g. (0.3 mol.) of 57% sodium hydride followed by an additional 400 ml. of dimethoxyethane. After stirring overnight the suspension is cooled to 4° C and a solution of 31.2 g. (0.27 mol.) of sulfamoyl chloride in 600 ml. of dimethoxyethane is added dropwise. The resulting suspension is stirred overnight at room temperature. The mixture is then filtered, the filtrate is concentrated and the residue washed with heptane. The residue is then chromatographed through SilicAR, CC-7 and eluted with 25% acetone-chloroform. The solid obtained after removel of the solvent is crystallized from a mixture of ethyl acetate-hexane-methylene chloride to afford 2-methyl-2-propyl-1,3-bis-O-sulfamyl-1,3-propanediol, m.p. 92°-94° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04075351 |
|---|
| Source dataset | uspto-grants-1978_02 |
|---|
| ORD ID | ord-cea2c23ec2ab4937893ebd86f8521c40 |
|---|
| Source note | uspto-grants-1978_02 |
|---|