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1-Bromo-3,7-dimethyloctane

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1-Bromo-3,7-dimethyloctane Basic information
Product Name:1-Bromo-3,7-dimethyloctane
Synonyms:3,7-DIMETHYLOCTYL BROMIDE;1-Bromo-3,7-dimethyloctane, technical grade;3,7-DIMETHYLOCTYL BROMIDE ---LIQUID, D20 1.07---;Perhydrogeranyl bromide;3,7-DiMethyl-1-broMooctane;Dihydrocitronellyl BroMide;Tetrahydrogeranyl BroMide;1-Bromo-3,7-dimethyloctane 96%
CAS:3383-83-3
MF:C10H21Br
MW:221.18
EINECS:
Product Categories:Building Blocks;Chemical Synthesis;Halogenated Hydrocarbons;Organic Building Blocks;Alkyl;Halogenated Hydrocarbons;Organic Building Blocks;Aliphatics
Mol File:3383-83-3.mol
1-Bromo-3,7-dimethyloctane Structure
1-Bromo-3,7-dimethyloctane Chemical Properties
Boiling point 135-140 °C10 mm Hg(lit.)
density 1.066 g/mL at 20 °C
refractive index n20/D 1.455(lit.)
Fp 210 °F
storage temp. 2-8°C
form clear liquid
color Colorless to Light yellow to Light orange
Optical Rotation0.45° (C=1.48 g/100ml,CHCL3)
InChI1S/C10H21Br/c1-9(2)5-4-6-10(3)7-8-11/h9-10H,4-8H2,1-3H3
InChIKeyVGSUDZKDSKCYJP-UHFFFAOYSA-N
SMILESCC(C)CCCC(C)CCBr
Safety Information
RIDADR UN 1993 / PGIII
WGK Germany 3
HS Code 2903.39.2050
Storage Class10 - Combustible liquids
MSDS Information
ProviderLanguage
SigmaAldrich English
1-Bromo-3,7-dimethyloctane Usage And Synthesis
Uses1-BroMo-3,7-diMethyloctane can be used in the preparation and properties of stimulus-responsive biodegradable polymers for biomedical uses.
Synthesis
3,7-DIMETHYL-1-OCTANOL

106-21-8

Octane, 1-bromo-3,7-dimethyl-, (3R)-

59965-20-7

The general procedure for the synthesis of (R)-1-bromo-3,7-dimethyloctane from 3,7-dimethyloctan-1-ol was as follows: concentrated sulfuric acid (17 mL) was slowly added to 48% hydrobromic acid (100 mL) under stirring conditions, followed by 3,7-dimethyloctan-1-ol (67 mL, 100 g). The reaction mixture was heated to 120-125 °C and maintained at this temperature for 3 hours. After completion of the reaction, the mixture was cooled and extracted with heptane (300 mL). The heptane layer was washed sequentially with dilute hydrochloric acid, water and sodium bicarbonate solution and concentrated after drying to give 81.5 g of oily crude product. This crude product was subjected to vacuum distillation at a bath temperature of 120-125 °C, and the fraction with a boiling point of 85-87 °C/10 mmHg was collected to afford the target product (R)-1-bromo-3,7-dimethyloctane in the form of colorless oil in a yield of 78.2 g in 100% yield. Mass spectrometry analysis showed molecular ion peaks m/z 220,222 (M+).

References[1] Patent: US8471035, 2013, B1. Location in patent: Page/Page column 9; 10
[2] Patent: US2018/273524, 2018, A1. Location in patent: Paragraph 0044
[3] Patent: EP2816053, 2014, A1. Location in patent: Paragraph 0352
[4] Patent: US9371353, 2016, B2. Location in patent: Page/Page column 73; 74; 75
[5] Helvetica Chimica Acta, 1981, vol. 64, # 4, p. 1158 - 1173
1-Bromo-3,7-dimethyloctane Preparation Products And Raw materials
Raw materials3,7-Dimethyl-1-octanol-->Sulfuric acid-->Hydrogen bromide
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