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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1762003Generated: October 28, 2026

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

https://huagongshe.com/reaction/1762003

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Nitro-2-isopropyl-1,3-propanediolHCID 143881—
Reactant(+-)(2R*,3RS,4R*)-3-Amino-3-methyl-2,4-pentanediol acetateHCID 53919029—
Product2-Amino-2-isopropyl-1,3-propanediol acetateHCID 1439124898%

Reaction Steps

Using the procedure in 5D, 2-isopropyl-2-nitro-1,3-propanediol (11A) gave a 98% yield of 2-amino-2-isopropyl-1,3-propanediol acetate 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 numberUS04829090
Source datasetuspto-grants-1989_05
ORD IDord-3bb3d3d7ccc94b43acd0b77127effb22
Source noteuspto-grants-1989_05