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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2413655Generated: October 29, 2026

2-Nitro-2-isopropyl-1,3-propanediol → 2-Amino-2-isopropyl-1,3-propanediol acetate

https://huagongshe.com/reaction/2413655

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Nitro-2-isopropyl-1,3-propanediolHCID 143881—
Reactant(+-)(2R*,3R*)-2-amino-2-methyl-1,3-butanediol acetateHCID 86741969—
Product2-Amino-2-isopropyl-1,3-propanediol acetateHCID 1439124898%

Reaction Steps

Using the procedure in 30E, 2-isopropyl-2-nitro-1,3-propanediol (52A) gave a 98% yield of 2-amino-2-isopropyl-1,3propanediol acetate.1/4H2O mp 155°-155.5°. H. S. Broadbent et al., J. Heterocyclic Chem., 13, 337 (1975) report the synthesis of this compound as the free base (mp 70°-72°)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04719049
Source datasetuspto-grants-1988_01
ORD IDord-85aec3bfd05f4b4e94c18ce9d32a1f15
Source noteuspto-grants-1988_01