HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → HCID 86735458, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | L-Serine | HCID 5951 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Serine, 2-(hydroxymethyl)- | HCID 439893 | — |
| Product | HCID 86735458 | HCID 86735458 | — |
Reaction Steps
In Scheme B serine is converted to 2-amino-3-hydroxy-2-hydroxymethylpropionic acid by reaction with aqueous sodium carbonate containing an excess of formaldehyde. From that point the synthesis is conducted as set out in Scheme A. However, it is preferable to activate 2-amino-3-hydroxy-2-hydroxymethylpropionic acid with 1-hydroxy benzotriazole to facilitate condensation with p- N,N-bis(2-chloroethyl)!phenylendediamine. The product, 2-amino-N- p-bis(2-chloroethyl)amino!phenyl-3-hydroxy-2-hydroxymethylpropionamide, is isolated as the hydrochloride salt. As in Scheme A, the hydrochloric acid may be replaced with those indicated acids.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04073807 |
| Source dataset | uspto-grants-1978_02 |
| ORD ID | ord-736dbf369e804335b061a7ef3dd9deeb |
| Source note | uspto-grants-1978_02 |